2,437 Clinical Research Coordinators jobs in the United States
Clinical Research Assistant
33084 Hollywood, Florida
Actalent
Posted 2 days ago
Job Viewed
Job Description
Clinical Research Assistant
MUST BE SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Nov 6, 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 SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Nov 6, 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 Assistant
33084 Hollywood, Florida
Actalent
Posted 2 days ago
Job Viewed
Job Description
Clinical Research Assistant (Bilingual - English/Spanish)Overview:
Supports Clinical Research Coordinators in executing clinical trials in compliance with ICH, GCP, protocol, and site policies. This entry-level role is ideal for individuals eager to grow into a CRC position.
Key Responsibilities:
+ Assist with patient visits, data entry, and study documentation.
+ Prepare lab kits, binders, and visit materials.
+ Maintain patient charts and study supply inventory.
+ Support CRCs with assessments (e.g., blood pressure, urine collection).
+ Communicate with participants, caregivers, vendors, and labs.
+ Help with scheduling, clerical tasks, and monitoring visits.
+ Perform daily delegated tasks related to study conduct.
Qualifications:
+ Bilingual in English and Spanish (required).
+ Strong organizational and communication skills.
+ Detail-oriented with a proactive mindset.
+ Comfortable using computers and electronic equipment.
+ Ability to stay calm and effective in fast-paced environments.
+ Interest in clinical research and study-specific indications.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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.
Supports Clinical Research Coordinators in executing clinical trials in compliance with ICH, GCP, protocol, and site policies. This entry-level role is ideal for individuals eager to grow into a CRC position.
Key Responsibilities:
+ Assist with patient visits, data entry, and study documentation.
+ Prepare lab kits, binders, and visit materials.
+ Maintain patient charts and study supply inventory.
+ Support CRCs with assessments (e.g., blood pressure, urine collection).
+ Communicate with participants, caregivers, vendors, and labs.
+ Help with scheduling, clerical tasks, and monitoring visits.
+ Perform daily delegated tasks related to study conduct.
Qualifications:
+ Bilingual in English and Spanish (required).
+ Strong organizational and communication skills.
+ Detail-oriented with a proactive mindset.
+ Comfortable using computers and electronic equipment.
+ Ability to stay calm and effective in fast-paced environments.
+ Interest in clinical research and study-specific indications.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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 Assistant
33084 Hollywood, Florida
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Description - Clinical Research Assistant
Direct Hire Opportunity
The Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
Required Skills & Qualifications
+ Bilingual in English and Spanish
+ Previous clinical research experience strongly preferred.
+ Phlebotomy experience is required.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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.
Direct Hire Opportunity
The Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
Required Skills & Qualifications
+ Bilingual in English and Spanish
+ Previous clinical research experience strongly preferred.
+ Phlebotomy experience is required.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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 Assistant
33126 Flagami, Florida
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Assistant
MUST BE SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Miami,FL.
Application Deadline
This position is anticipated to close on Oct 27, 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 SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Miami,FL.
Application Deadline
This position is anticipated to close on Oct 27, 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 Assistant
33084 Hollywood, Florida
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Assistant
MUST BE SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 27, 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 SPANISH-SPEAKING
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 27, 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 Assistant
33084 Hollywood, Florida
Actalent
Posted 5 days ago
Job Viewed
Job Description
Job Summary:
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
+ Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
+ 1-2 years of experience in a Medical Assistant role - EKGs, vitals, blood draw experience
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Schedule: Monday - Friday 8:00 am - 4:30 pm + Occasional Saturdays
Pay and Benefits
The pay range for this position is $20.00 - $22.00/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 Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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.
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection.
+ Communicating with study participants, caregivers, third-party vendors, and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
+ 1-2 years of experience in a Medical Assistant role - EKGs, vitals, blood draw experience
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Schedule: Monday - Friday 8:00 am - 4:30 pm + Occasional Saturdays
Pay and Benefits
The pay range for this position is $20.00 - $22.00/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 Hollywood,FL.
Application Deadline
This position is anticipated to close on Oct 31, 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.
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5
Clinical Research Assistant
11040 New Hyde Park, New York
Northwell Health
Posted 2 days ago
Job Viewed
Job Description
**Req Number**
Job Description
Participates and assists in research and academic activities. Collaborates with all members of the research program as well as nursing, physician, house staff, and ancillary staff related to academic activities of the department.
Job Responsibility
+ Participates in research activities; assists the research team in identifying appropriate potential candidates for research protocols and preparation of research documents.
+ Interfaces and collaborates with the Medical Records and the auxiliary department as necessary.
+ Retrieves academic/research articles from library; maintains organized filing of documents.
+ Liaises between the department and other Institutional staff, as appropriate.
+ Supports staff in preparing for academic/research meetings and presentations including coordination with other departments.
+ Assists in the drafting of research proposals; facilitates mass mailing of research documents/letters, as appropriate.
+ Performs literature searches as necessary.
+ Acts as a liaison between researchers and the medical library personnel; interfaces and collaborates with members of the healthcare team.
+ Interacts with departments and staff.
+ Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions.
Job Qualification
+ High School Diploma or equivalent required.
+ Bachelor's degree, preferred
+ Some experience in a research environment, preferred
+ Experience with human subject research, preferred
*Additional Salary Detail
The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future.When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).
The salary range for this position is $39,290-$59,800/year
It is Northwell Health's policy to provide equal employment opportunity and treat all applicants and employees equally regardless of their age, race, creed/religion, color, national origin, immigration status or citizenship status, sexual orientation, military or veteran status, sex/gender, gender identity, gender expression, disability, pregnancy, genetic information or genetic predisposition or carrier status, marital or familial status, partnership status, victim of domestic violence, sexual or other reproductive health decisions, or other characteristics protected by applicable law.
Job Description
Participates and assists in research and academic activities. Collaborates with all members of the research program as well as nursing, physician, house staff, and ancillary staff related to academic activities of the department.
Job Responsibility
+ Participates in research activities; assists the research team in identifying appropriate potential candidates for research protocols and preparation of research documents.
+ Interfaces and collaborates with the Medical Records and the auxiliary department as necessary.
+ Retrieves academic/research articles from library; maintains organized filing of documents.
+ Liaises between the department and other Institutional staff, as appropriate.
+ Supports staff in preparing for academic/research meetings and presentations including coordination with other departments.
+ Assists in the drafting of research proposals; facilitates mass mailing of research documents/letters, as appropriate.
+ Performs literature searches as necessary.
+ Acts as a liaison between researchers and the medical library personnel; interfaces and collaborates with members of the healthcare team.
+ Interacts with departments and staff.
+ Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions.
Job Qualification
+ High School Diploma or equivalent required.
+ Bachelor's degree, preferred
+ Some experience in a research environment, preferred
+ Experience with human subject research, preferred
*Additional Salary Detail
The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future.When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).
The salary range for this position is $39,290-$59,800/year
It is Northwell Health's policy to provide equal employment opportunity and treat all applicants and employees equally regardless of their age, race, creed/religion, color, national origin, immigration status or citizenship status, sexual orientation, military or veteran status, sex/gender, gender identity, gender expression, disability, pregnancy, genetic information or genetic predisposition or carrier status, marital or familial status, partnership status, victim of domestic violence, sexual or other reproductive health decisions, or other characteristics protected by applicable law.
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6
Clinical Research Assistant
08757 Toms River, New Jersey
Actalent
Posted today
Job Viewed
Job Description
Description
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
MUST HAVES
Willing to learn phlebotomy; career-minded toward CRC path. (must be comfortable with patient care and vitals/specimens)
Eager to learn and grow
- Creating and maintaining patient charts for all assigned studies.
- Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
- Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
- Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
- Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
- Communicating with study participants, caregivers, third party vendors and laboratories as needed.
- Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
- Aiding Coordinators in the facilitation of study monitoring visits.
- Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
- Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
Soft Skills: willingness to learn, eager, career-minded
NICE TO HAVE
Bachelors degree in sciences/psych/bio
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Toms River,NJ.
Application Deadline
This position is anticipated to close on Oct 31, 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.
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
MUST HAVES
Willing to learn phlebotomy; career-minded toward CRC path. (must be comfortable with patient care and vitals/specimens)
Eager to learn and grow
- Creating and maintaining patient charts for all assigned studies.
- Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
- Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
- Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
- Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
- Communicating with study participants, caregivers, third party vendors and laboratories as needed.
- Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
- Aiding Coordinators in the facilitation of study monitoring visits.
- Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
- Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
Soft Skills: willingness to learn, eager, career-minded
NICE TO HAVE
Bachelors degree in sciences/psych/bio
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Toms River,NJ.
Application Deadline
This position is anticipated to close on Oct 31, 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 Assistant
08054 Mount Laurel, New Jersey
Actalent
Posted 4 days ago
Job Viewed
Job Description
Clinical Research Assistant
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Mount Laurel,NJ.
Application Deadline
This position is anticipated to close on Oct 27, 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.
Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Description
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
+ Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
+ Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Additional Skills & Qualifications
+ High School Diploma
+ Interest in and knowledge of specific study indications.
+ Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
+ Skilled in organization and record maintenance.
+ Skilled in developing and maintaining effective working relationships with supervisors and co- workers.
+ Strong personal initiative and attention to detail.
+ Ability to react calmly and effectively in emergency situations.
+ Ability to interpret, adapt and apply guidelines and procedures.
+ Ability to clearly communicate both orally and verbally.
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Mount Laurel,NJ.
Application Deadline
This position is anticipated to close on Oct 27, 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 Assistant
08053 Marlton, New Jersey
Actalent
Posted 4 days ago
Job Viewed
Job Description
Job Description - Clinical Research Assistant
Direct Hire Opportunity
The Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
Required Skills & Qualifications
+ Previous clinical research experience strongly preferred.
+ Phlebotomy experience is required.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Evesham,NJ.
Application Deadline
This position is anticipated to close on Oct 31, 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.
Direct Hire Opportunity
The Clinical Research Assistant will provide direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Job Duties:
+ Creating and maintaining patient charts for all assigned studies.
+ Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
+ Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
+ Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
+ Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.
+ Communicating with study participants, caregivers, third party vendors and laboratories as needed.
+ Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
+ Aiding Coordinators in the facilitation of study monitoring visits.
Required Skills & Qualifications
+ Previous clinical research experience strongly preferred.
+ Phlebotomy experience is required.
Pay and Benefits
The pay range for this position is $ - $ /yr.
Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.
Workplace Type
This is a fully onsite position in Evesham,NJ.
Application Deadline
This position is anticipated to close on Oct 31, 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