4,063 Clinical Research Associates jobs in the United States
Clinical Research Coordinator
37621 Bristol, Tennessee
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Coordinator
MUST be local to Bristol, TN as interviews will be onsite!
MUST have patience facing Clinical Research experience
Contract
6 months with the potential for extension
Clinical Research Coordinator
+ Recruits and consents research participants.
+ Conducts telephone or in-person interviews with participants,
+ including screening for eligibility.
+ Performs follow-up by telephone, e-mail, and/or mail with
+ study participants.
+ Prepares, mails, and processes questionnaires and other study
+ correspondence.
+ Assists in tracking study participants using MS Excel.
+ Keeps accurate and detailed records and files of work.
Qualifications
+ 1+ year of Clinical Research Coordinator (CRC) experience
+ Experience with chart review and patient recruitment
+ Knowledge of EDC and EMR systems
+ Understanding of clinical research and Good Clinical Practice
+ (GCP)
+ Experience in pre-screening patients
+ High school diploma or General Education Development (GED)
+ required
Pay and Benefits
The pay range for this position is $25.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bristol,TN.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
MUST be local to Bristol, TN as interviews will be onsite!
MUST have patience facing Clinical Research experience
Contract
6 months with the potential for extension
Clinical Research Coordinator
+ Recruits and consents research participants.
+ Conducts telephone or in-person interviews with participants,
+ including screening for eligibility.
+ Performs follow-up by telephone, e-mail, and/or mail with
+ study participants.
+ Prepares, mails, and processes questionnaires and other study
+ correspondence.
+ Assists in tracking study participants using MS Excel.
+ Keeps accurate and detailed records and files of work.
Qualifications
+ 1+ year of Clinical Research Coordinator (CRC) experience
+ Experience with chart review and patient recruitment
+ Knowledge of EDC and EMR systems
+ Understanding of clinical research and Good Clinical Practice
+ (GCP)
+ Experience in pre-screening patients
+ High school diploma or General Education Development (GED)
+ required
Pay and Benefits
The pay range for this position is $25.00 - $30.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bristol,TN.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
0
Clinical Research Coordinator
95351 Long Barn, California
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Coordinator
Job Description
We are seeking an experienced Clinical Research Coordinator with a minimum of 3 years of clinical research experience. The ideal candidate will have a proven ability to communicate directly with Principal Investigators (PIs) and sponsors. This role requires a demonstrated initiative and independence, as it is a solo position at the site, working alongside a nurse lead.
Responsibilities
* Perform regulatory tasks, including IRB submissions.
* Engage in sponsor correspondence, excluding budget and contracting.
* Oversee the informed consent process.
* Schedule standard-of-care procedures.
* Manage Investigational Product (IP) accountability.
* Collaborate with local nurses for blood draws.
* Maintain direct communication with investigators.
* Actively manage client engagement.
Essential Skills
* Pre-screening patients
* Clinical research
* Oncology expertise
* Clinical trial management
* Good Clinical Practice (GCP)
* IRB knowledge
* Regulatory experience
* Patient recruitment
* Data entry proficiency
* Electronic Data Capture (EDC)
* National Cancer Institute (NCI) trial involvement
Additional Skills & Qualifications
* Experience with NCI trials and federally funded research.
* Prior involvement in research funded by NCORP grants.
Work Environment
This position is a solo coordinator role onsite, with occasional support from the site manager. The role requires a high degree of independence and the ability to work autonomously. The work environment is mission-driven, focusing on a patient-first approach within a growing research portfolio.
Pay and Benefits
The pay range for this position is $35.00 - $39.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Modesto,CA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
Job Description
We are seeking an experienced Clinical Research Coordinator with a minimum of 3 years of clinical research experience. The ideal candidate will have a proven ability to communicate directly with Principal Investigators (PIs) and sponsors. This role requires a demonstrated initiative and independence, as it is a solo position at the site, working alongside a nurse lead.
Responsibilities
* Perform regulatory tasks, including IRB submissions.
* Engage in sponsor correspondence, excluding budget and contracting.
* Oversee the informed consent process.
* Schedule standard-of-care procedures.
* Manage Investigational Product (IP) accountability.
* Collaborate with local nurses for blood draws.
* Maintain direct communication with investigators.
* Actively manage client engagement.
Essential Skills
* Pre-screening patients
* Clinical research
* Oncology expertise
* Clinical trial management
* Good Clinical Practice (GCP)
* IRB knowledge
* Regulatory experience
* Patient recruitment
* Data entry proficiency
* Electronic Data Capture (EDC)
* National Cancer Institute (NCI) trial involvement
Additional Skills & Qualifications
* Experience with NCI trials and federally funded research.
* Prior involvement in research funded by NCORP grants.
Work Environment
This position is a solo coordinator role onsite, with occasional support from the site manager. The role requires a high degree of independence and the ability to work autonomously. The work environment is mission-driven, focusing on a patient-first approach within a growing research portfolio.
Pay and Benefits
The pay range for this position is $35.00 - $39.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Modesto,CA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
View Now
1
Clinical Research Coordinator
28111 Monroe, North Carolina
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator
Duration: Open-ended contract (average duration 3-6 months)
Job Type: 30 hours per week (Monday-Friday) - during normal business hours
Start Date: ASAP
Job Description:
We are seeking an onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Vaccine clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study.
Key Responsibilities:
Medical Record Review: Conduct thorough reviews of patient medical records.
Participant Screening: Perform phone screenings or prescreen participants for eligibility.
Informed Consent: Obtain informed consent from trial participants.
Medical Record Retrieval: Obtain necessary medical records for the study.
Community Outreach: Visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.
Referral Physician Networking: Building relationships between clinical researchers and community physicians to facilitate patient recruitment for clinical trials
Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.
General Support: Assist with any other study-related efforts as deemed necessary by the site.
Qualifications:
+ Minimum of two years of experience as a Clinical Research Coordinator
+ Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Monroe,NC.
Application Deadline
This position is anticipated to close on Sep 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Duration: Open-ended contract (average duration 3-6 months)
Job Type: 30 hours per week (Monday-Friday) - during normal business hours
Start Date: ASAP
Job Description:
We are seeking an onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Vaccine clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study.
Key Responsibilities:
Medical Record Review: Conduct thorough reviews of patient medical records.
Participant Screening: Perform phone screenings or prescreen participants for eligibility.
Informed Consent: Obtain informed consent from trial participants.
Medical Record Retrieval: Obtain necessary medical records for the study.
Community Outreach: Visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.
Referral Physician Networking: Building relationships between clinical researchers and community physicians to facilitate patient recruitment for clinical trials
Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.
General Support: Assist with any other study-related efforts as deemed necessary by the site.
Qualifications:
+ Minimum of two years of experience as a Clinical Research Coordinator
+ Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Monroe,NC.
Application Deadline
This position is anticipated to close on Sep 9, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
2
Clinical Research Coordinator
91116 Pasadena, California
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Coordinator
Overview:
Seeking an experienced Clinical Research Coordinator to manage multiple clinical trials, ensure protocol compliance, and support patient engagement throughout the study lifecycle.
Key Responsibilities:
+ Manage 6-8 clinical trials
+ Conduct patient screening, informed consent, and study visits
+ Maintain accurate documentation and case report forms
+ Monitor lab results and report adverse events
+ Train staff on protocol updates
Qualifications:
+ RN/LVN or Bachelor's degree
+ 5+ years of clinical research experience
+ Knowledge of FDA, ICH, and GCP guidelines
+ Experience with Phase I-IV trials
+ BCLS certification required
+ IATA certification
Pay and Benefits
The pay range for this position is $30.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Pasadena,CA.
Application Deadline
This position is anticipated to close on Sep 11, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Overview:
Seeking an experienced Clinical Research Coordinator to manage multiple clinical trials, ensure protocol compliance, and support patient engagement throughout the study lifecycle.
Key Responsibilities:
+ Manage 6-8 clinical trials
+ Conduct patient screening, informed consent, and study visits
+ Maintain accurate documentation and case report forms
+ Monitor lab results and report adverse events
+ Train staff on protocol updates
Qualifications:
+ RN/LVN or Bachelor's degree
+ 5+ years of clinical research experience
+ Knowledge of FDA, ICH, and GCP guidelines
+ Experience with Phase I-IV trials
+ BCLS certification required
+ IATA certification
Pay and Benefits
The pay range for this position is $30.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Pasadena,CA.
Application Deadline
This position is anticipated to close on Sep 11, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
3
Clinical Research Coordinator
70402 Hammond, Louisiana
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator
Job Description
We are seeking a dedicated Clinical Research Coordinator to join a cardiology study in Hammond, LA. This role involves managing clinical trials, ensuring data accuracy, and facilitating patient recruitment. The contract duration is until November 2025 with potential for extension.
Responsibilities
+ Perform data entry and maintain accurate records.
+ Resolve queries related to clinical trials.
+ Conduct community outreach to support patient recruitment.
+ Coordinate and manage all aspects of clinical research activities.
Essential Skills
+ Minimum of 2 years' experience as a Clinical Research Coordinator.
+ Minimum of 2 years' experience in clinical trials and query resolution.
+ Proficient in electronic data capture (EDC) systems.
+ Strong skills in community outreach, patient recruitment and data entry.
Additional Skills & Qualifications
+ Previous clinical research experience is required.
Work Environment
The position operates during normal business hours in a fast-paced environment that demands attention to detail.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hammond,LA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Job Description
We are seeking a dedicated Clinical Research Coordinator to join a cardiology study in Hammond, LA. This role involves managing clinical trials, ensuring data accuracy, and facilitating patient recruitment. The contract duration is until November 2025 with potential for extension.
Responsibilities
+ Perform data entry and maintain accurate records.
+ Resolve queries related to clinical trials.
+ Conduct community outreach to support patient recruitment.
+ Coordinate and manage all aspects of clinical research activities.
Essential Skills
+ Minimum of 2 years' experience as a Clinical Research Coordinator.
+ Minimum of 2 years' experience in clinical trials and query resolution.
+ Proficient in electronic data capture (EDC) systems.
+ Strong skills in community outreach, patient recruitment and data entry.
Additional Skills & Qualifications
+ Previous clinical research experience is required.
Work Environment
The position operates during normal business hours in a fast-paced environment that demands attention to detail.
Pay and Benefits
The pay range for this position is $25.00 - $35.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hammond,LA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
4
Clinical Research Coordinator
95397 Long Barn, California
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Coordinator Job Description
We are seeking an experienced Clinical Research Coordinator with a minimum of 3 years of clinical research experience. The ideal candidate will have a proven ability to communicate directly with Principal Investigators (PIs) and sponsors. This role requires a demonstrated initiative and independence, as it is a solo position at the site, working alongside a nurse lead.
Responsibilities
+ Perform regulatory tasks, including IRB submissions.
+ Engage in sponsor correspondence, excluding budget and contracting.
+ Oversee the informed consent process.
+ Schedule standard-of-care procedures.
+ Manage Investigational Product (IP) accountability.
+ Collaborate with local nurses for blood draws.
+ Maintain direct communication with investigators.
+ Actively manage client engagement.
Essential Skills
+ Pre-screening patients
+ Clinical research
+ Oncology expertise
+ Clinical trial management
+ Good Clinical Practice (GCP)
+ IRB knowledge
+ Regulatory experience
+ Patient recruitment
+ Data entry proficiency
+ Electronic Data Capture (EDC)
+ National Cancer Institute (NCI) trial involvement
Additional Skills & Qualifications
+ Experience with NCI trials and federally funded research.
+ Prior involvement in research funded by NCORP grants.
Work Environment
This position is a solo coordinator role onsite, with occasional support from the site manager. The role requires a high degree of independence and the ability to work autonomously. The work environment is mission-driven, focusing on a patient-first approach within a growing research portfolio.
Pay and Benefits
The pay range for this position is $35.00 - $39.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Modesto,CA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
We are seeking an experienced Clinical Research Coordinator with a minimum of 3 years of clinical research experience. The ideal candidate will have a proven ability to communicate directly with Principal Investigators (PIs) and sponsors. This role requires a demonstrated initiative and independence, as it is a solo position at the site, working alongside a nurse lead.
Responsibilities
+ Perform regulatory tasks, including IRB submissions.
+ Engage in sponsor correspondence, excluding budget and contracting.
+ Oversee the informed consent process.
+ Schedule standard-of-care procedures.
+ Manage Investigational Product (IP) accountability.
+ Collaborate with local nurses for blood draws.
+ Maintain direct communication with investigators.
+ Actively manage client engagement.
Essential Skills
+ Pre-screening patients
+ Clinical research
+ Oncology expertise
+ Clinical trial management
+ Good Clinical Practice (GCP)
+ IRB knowledge
+ Regulatory experience
+ Patient recruitment
+ Data entry proficiency
+ Electronic Data Capture (EDC)
+ National Cancer Institute (NCI) trial involvement
Additional Skills & Qualifications
+ Experience with NCI trials and federally funded research.
+ Prior involvement in research funded by NCORP grants.
Work Environment
This position is a solo coordinator role onsite, with occasional support from the site manager. The role requires a high degree of independence and the ability to work autonomously. The work environment is mission-driven, focusing on a patient-first approach within a growing research portfolio.
Pay and Benefits
The pay range for this position is $35.00 - $39.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Modesto,CA.
Application Deadline
This position is anticipated to close on Sep 8, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
5
Clinical Research Coordinator
19107 Philadelphia, Pennsylvania
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator - Drug or Device study experience required
Job Description
Join our dynamic research team to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work closely with study physicians, research coordinators, project managers, and other research staff to advance our research mission within a vibrant Division.
Responsibilities
* Assist with study coordination and recruitment for various research projects.
* Work directly with study physicians, research coordinators, project managers, and other research staff.
* Perform screening visits and consent participants for studies.
* Process and ship laboratory samples.
* Enter data into databases accurately and efficiently.
* Escort participants to other testing and procedure areas.
Essential Skills
* Experience in clinical research, patient enrollment, and recruitment.
* Proficiency in chart review and data entry.
* Ability to pre-screen patients effectively.
* Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB), and Electronic Data Capture (EDC) systems.
Additional Skills & Qualifications
* 1-2 years of related experience or an equivalent combination of education and experience.
Work Environment
This role offers flexibility with work-from-home options: the first week is on-site, with one day of remote work available during the first four months. After establishing your role, two days of remote work are possible, as long as it does not interfere with departmental operations. The work location is conveniently situated near public transportation options, including PATCO and SEPTA, with parking available. The team is diverse and well-supported, fostering a collaborative and fulfilling work environment. You will work on high-profile studies, including drug trials for movement disorders such as Parkinson's disease, within a recognized Center of Excellence. The opportunity is both challenging and rewarding, with the chance to contribute significantly to research that impacts lives.
Job Type & Location
This is a Contract to Hire position based out of Philadelphia, Pennsylvania.
Pay and Benefits
The pay range for this position is $25.00 - $29.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Philadelphia,PA.
Application Deadline
This position is anticipated to close on Sep 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
Job Description
Join our dynamic research team to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work closely with study physicians, research coordinators, project managers, and other research staff to advance our research mission within a vibrant Division.
Responsibilities
* Assist with study coordination and recruitment for various research projects.
* Work directly with study physicians, research coordinators, project managers, and other research staff.
* Perform screening visits and consent participants for studies.
* Process and ship laboratory samples.
* Enter data into databases accurately and efficiently.
* Escort participants to other testing and procedure areas.
Essential Skills
* Experience in clinical research, patient enrollment, and recruitment.
* Proficiency in chart review and data entry.
* Ability to pre-screen patients effectively.
* Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB), and Electronic Data Capture (EDC) systems.
Additional Skills & Qualifications
* 1-2 years of related experience or an equivalent combination of education and experience.
Work Environment
This role offers flexibility with work-from-home options: the first week is on-site, with one day of remote work available during the first four months. After establishing your role, two days of remote work are possible, as long as it does not interfere with departmental operations. The work location is conveniently situated near public transportation options, including PATCO and SEPTA, with parking available. The team is diverse and well-supported, fostering a collaborative and fulfilling work environment. You will work on high-profile studies, including drug trials for movement disorders such as Parkinson's disease, within a recognized Center of Excellence. The opportunity is both challenging and rewarding, with the chance to contribute significantly to research that impacts lives.
Job Type & Location
This is a Contract to Hire position based out of Philadelphia, Pennsylvania.
Pay and Benefits
The pay range for this position is $25.00 - $29.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Philadelphia,PA.
Application Deadline
This position is anticipated to close on Sep 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
View Now
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6
Clinical Research Coordinator
19133 Philadelphia, Pennsylvania
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator - Drug or Device study experience required
Job Description
Join our dynamic research team to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work closely with study physicians, research coordinators, project managers, and other research staff to advance our research mission within a vibrant Division.
Responsibilities
+ Assist with study coordination and recruitment for various research projects.
+ Work directly with study physicians, research coordinators, project managers, and other research staff.
+ Perform screening visits and consent participants for studies.
+ Process and ship laboratory samples.
+ Enter data into databases accurately and efficiently.
+ Escort participants to other testing and procedure areas.
Essential Skills
+ Experience in clinical research, patient enrollment, and recruitment.
+ Proficiency in chart review and data entry.
+ Ability to pre-screen patients effectively.
+ Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB), and Electronic Data Capture (EDC) systems.
Additional Skills & Qualifications
+ 1-2 years of related experience or an equivalent combination of education and experience.
Work Environment
This role offers flexibility with work-from-home options: the first week is on-site, with one day of remote work available during the first four months. After establishing your role, two days of remote work are possible, as long as it does not interfere with departmental operations. The work location is conveniently situated near public transportation options, including PATCO and SEPTA, with parking available. The team is diverse and well-supported, fostering a collaborative and fulfilling work environment. You will work on high-profile studies, including drug trials for movement disorders such as Parkinson's disease, within a recognized Center of Excellence. The opportunity is both challenging and rewarding, with the chance to contribute significantly to research that impacts lives.
Job Type & Location
This is a Contract to Hire position based out of Philadelphia, Pennsylvania.
Pay and Benefits
The pay range for this position is $25.00 - $29.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Philadelphia,PA.
Application Deadline
This position is anticipated to close on Sep 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Job Description
Join our dynamic research team to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work closely with study physicians, research coordinators, project managers, and other research staff to advance our research mission within a vibrant Division.
Responsibilities
+ Assist with study coordination and recruitment for various research projects.
+ Work directly with study physicians, research coordinators, project managers, and other research staff.
+ Perform screening visits and consent participants for studies.
+ Process and ship laboratory samples.
+ Enter data into databases accurately and efficiently.
+ Escort participants to other testing and procedure areas.
Essential Skills
+ Experience in clinical research, patient enrollment, and recruitment.
+ Proficiency in chart review and data entry.
+ Ability to pre-screen patients effectively.
+ Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB), and Electronic Data Capture (EDC) systems.
Additional Skills & Qualifications
+ 1-2 years of related experience or an equivalent combination of education and experience.
Work Environment
This role offers flexibility with work-from-home options: the first week is on-site, with one day of remote work available during the first four months. After establishing your role, two days of remote work are possible, as long as it does not interfere with departmental operations. The work location is conveniently situated near public transportation options, including PATCO and SEPTA, with parking available. The team is diverse and well-supported, fostering a collaborative and fulfilling work environment. You will work on high-profile studies, including drug trials for movement disorders such as Parkinson's disease, within a recognized Center of Excellence. The opportunity is both challenging and rewarding, with the chance to contribute significantly to research that impacts lives.
Job Type & Location
This is a Contract to Hire position based out of Philadelphia, Pennsylvania.
Pay and Benefits
The pay range for this position is $25.00 - $29.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Philadelphia,PA.
Application Deadline
This position is anticipated to close on Sep 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
7
Clinical Research Coordinator
08901 New Brunswick, New Jersey
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research CoordinatorJob Description
We are seeking a Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various committees, preparing study tools, and ensuring compliance with study protocols.
Responsibilities
+ Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and documentation are in place.
+ Prepare study tools such as binders, medication diaries, eligibility checklists, and flow sheets.
+ Collaborate with Research Nurse Clinicians and physicians to review patient charts and confirm protocol eligibility.
+ Ensure informed consent forms are obtained and documented properly.
+ Register consented research patients with study sponsors and input data into the clinical trials database.
+ Maintain comprehensive research records for all patients enrolled in clinical trials.
+ Assist in grading adverse events and complete necessary forms for serious or unexpected adverse events.
+ Provide regular reports to study group members and Principal Investigators.
+ Serve as a liaison with study sponsors, schedule monitoring visits, and respond to queries.
+ Ensure studies are conducted according to treatment plans and Good Clinical Practice (GCP) guidelines.
Essential Skills
+ 1-3 years of experience as a Clinical Research Coordinator.
+ Proficiency in clinical research, oncology, and informed consent processes.
+ Ability to recruit, enroll, and manage source documents for patients.
+ Experience with software programs such as Excel®, Word®, and Access®.
+ Strong organizational, communication, and interpersonal skills.
Additional Skills & Qualifications
+ Bachelor's Degree required.
+ Detail-oriented with the ability to maximize resources and be resourceful.
+ Commitment to high standards of professional excellence and accountability.
Work Environment
This position is part of a Clinical Operations team comprising 40 FTEs across various disease-specific groups, including breast, lung, phase 1, and GI. The team operates in multiple sites, including Newark, with a goal to enroll 5,000 subjects per year across 300 active trials. The work environment includes collaboration with RA, QA, Informatics, Education, and Finance departments, aiming for a long-term goal of 2,500 active subjects across all phases of adult and pediatric trials.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $30.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
We are seeking a Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various committees, preparing study tools, and ensuring compliance with study protocols.
Responsibilities
+ Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and documentation are in place.
+ Prepare study tools such as binders, medication diaries, eligibility checklists, and flow sheets.
+ Collaborate with Research Nurse Clinicians and physicians to review patient charts and confirm protocol eligibility.
+ Ensure informed consent forms are obtained and documented properly.
+ Register consented research patients with study sponsors and input data into the clinical trials database.
+ Maintain comprehensive research records for all patients enrolled in clinical trials.
+ Assist in grading adverse events and complete necessary forms for serious or unexpected adverse events.
+ Provide regular reports to study group members and Principal Investigators.
+ Serve as a liaison with study sponsors, schedule monitoring visits, and respond to queries.
+ Ensure studies are conducted according to treatment plans and Good Clinical Practice (GCP) guidelines.
Essential Skills
+ 1-3 years of experience as a Clinical Research Coordinator.
+ Proficiency in clinical research, oncology, and informed consent processes.
+ Ability to recruit, enroll, and manage source documents for patients.
+ Experience with software programs such as Excel®, Word®, and Access®.
+ Strong organizational, communication, and interpersonal skills.
Additional Skills & Qualifications
+ Bachelor's Degree required.
+ Detail-oriented with the ability to maximize resources and be resourceful.
+ Commitment to high standards of professional excellence and accountability.
Work Environment
This position is part of a Clinical Operations team comprising 40 FTEs across various disease-specific groups, including breast, lung, phase 1, and GI. The team operates in multiple sites, including Newark, with a goal to enroll 5,000 subjects per year across 300 active trials. The work environment includes collaboration with RA, QA, Informatics, Education, and Finance departments, aiming for a long-term goal of 2,500 active subjects across all phases of adult and pediatric trials.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $30.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
View Now
8
Clinical Research Coordinator
08903 New Brunswick, New Jersey
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator
Job Description
We are seeking a Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various committees, preparing study tools, and ensuring compliance with study protocols.
Responsibilities
* Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and documentation are in place.
* Prepare study tools such as binders, medication diaries, eligibility checklists, and flow sheets.
* Collaborate with Research Nurse Clinicians and physicians to review patient charts and confirm protocol eligibility.
* Ensure informed consent forms are obtained and documented properly.
* Register consented research patients with study sponsors and input data into the clinical trials database.
* Maintain comprehensive research records for all patients enrolled in clinical trials.
* Assist in grading adverse events and complete necessary forms for serious or unexpected adverse events.
* Provide regular reports to study group members and Principal Investigators.
* Serve as a liaison with study sponsors, schedule monitoring visits, and respond to queries.
* Ensure studies are conducted according to treatment plans and Good Clinical Practice (GCP) guidelines.
Essential Skills
* 1-3 years of experience as a Clinical Research Coordinator.
* Proficiency in clinical research, oncology, and informed consent processes.
* Ability to recruit, enroll, and manage source documents for patients.
* Experience with software programs such as Excel, Word, and Access.
* Strong organizational, communication, and interpersonal skills.
Additional Skills & Qualifications
* Bachelor's Degree required.
* Detail-oriented with the ability to maximize resources and be resourceful.
* Commitment to high standards of professional excellence and accountability.
Work Environment
This position is part of a Clinical Operations team comprising 40 FTEs across various disease-specific groups, including breast, lung, phase 1, and GI. The team operates in multiple sites, including Newark, with a goal to enroll 5,000 subjects per year across 300 active trials. The work environment includes collaboration with RA, QA, Informatics, Education, and Finance departments, aiming for a long-term goal of 2,500 active subjects across all phases of adult and pediatric trials.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $30.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
Job Description
We are seeking a Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various committees, preparing study tools, and ensuring compliance with study protocols.
Responsibilities
* Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and documentation are in place.
* Prepare study tools such as binders, medication diaries, eligibility checklists, and flow sheets.
* Collaborate with Research Nurse Clinicians and physicians to review patient charts and confirm protocol eligibility.
* Ensure informed consent forms are obtained and documented properly.
* Register consented research patients with study sponsors and input data into the clinical trials database.
* Maintain comprehensive research records for all patients enrolled in clinical trials.
* Assist in grading adverse events and complete necessary forms for serious or unexpected adverse events.
* Provide regular reports to study group members and Principal Investigators.
* Serve as a liaison with study sponsors, schedule monitoring visits, and respond to queries.
* Ensure studies are conducted according to treatment plans and Good Clinical Practice (GCP) guidelines.
Essential Skills
* 1-3 years of experience as a Clinical Research Coordinator.
* Proficiency in clinical research, oncology, and informed consent processes.
* Ability to recruit, enroll, and manage source documents for patients.
* Experience with software programs such as Excel, Word, and Access.
* Strong organizational, communication, and interpersonal skills.
Additional Skills & Qualifications
* Bachelor's Degree required.
* Detail-oriented with the ability to maximize resources and be resourceful.
* Commitment to high standards of professional excellence and accountability.
Work Environment
This position is part of a Clinical Operations team comprising 40 FTEs across various disease-specific groups, including breast, lung, phase 1, and GI. The team operates in multiple sites, including Newark, with a goal to enroll 5,000 subjects per year across 300 active trials. The work environment includes collaboration with RA, QA, Informatics, Education, and Finance departments, aiming for a long-term goal of 2,500 active subjects across all phases of adult and pediatric trials.
Job Type & Location
This is a Contract to Hire position based out of New Brunswick, New Jersey.
Pay and Benefits
The pay range for this position is $30.00 - $32.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
* Health Spending Account (HSA)
* Transportation benefits
* Employee Assistance Program
* Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Sep 5, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.
View Now
9