9,906 Trial Coordination jobs in the United States

Clinical Study Specialist
Job Description
As a Clinical Trial Coordinator, you will play a pivotal role in the initiation and activation of new clinical trial protocols, ensuring adherence to protocol requirements and facilitating effective patient care throughout the trial process. You will collaborate with multidisciplinary teams to overcome obstacles and promote a seamless study experience.
Responsibilities
+ Collaborate with the Protocol Activation office to initiate and activate clinical trial protocols using the Study-start up task list.
+ Prepare and review study tools, such as study binders, medication diaries, eligibility checklists, and flow sheets.
+ Verify Scientific Review Board, Institutional Review Board, data collection plans, and finance/contract approvals prior to study activation.
+ Review protocols and collect logistical, educational, and financial feedback to identify and resolve potential obstacles.
+ Perform protocol-related nursing education to facilitate safe, effective care for enrolled patients.
+ Translate finalized protocol treatment plans into sample orders.
+ Collaborate with the clinical research team for timely prescreening of potential subjects and review patient charts for protocol eligibility.
+ Ensure informed consent is obtained and documented according to IRB, GCP, and institutional policies.
+ Provide back-up support to register consented research patients with study sponsors and maintain clinical trials database.
+ Serve as a resource for Clinical Trial Billing Information related to assigned studies.
+ Actively identify and address challenges with protocol adherence and execution.
+ Coordinate protocol-specific procedures and treatments for study patients across disciplines and sites of care.
+ Essential Skills
+ Clinical Research Coordinator experience, particularly in oncology.
+ Proficiency in informed consent processes, patient recruitment, and enrollment.
+ Experience with source documents and screening of patients.
+ Ability to coordinate studies and communicate effectively with patients.
+ 2-3 years of clinical research coordination experience.
Pay and Benefits
The pay range for this position is $33.00 - $38.00/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 hybrid position in New Brunswick,NJ.
Application Deadline
This position is anticipated to close on Sep 16, 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 Title: Study Coordinator
Job Description
Engage in human subject research, focusing on wearable devices in an exercise setting. Monitor participants, collect data, and ensure the proper setup and functioning of technology products throughout the study sessions. Facilitate participant interaction and data collection according to established protocols.
Responsibilities
+ Conduct research with human participants using wearable devices.
+ Consent participants, and take necessary vitals and measurements such as height, weight, and EKG throughout sessions.
+ Ensure participants are properly set up with devices and monitoring equipment.
+ Observe participants using devices during various activities according to protocol.
+ Ensure data monitoring and collection are functioning properly, both through equipment and manually.
+ Guide participants throughout the study sessions, which can last up to 2.5 hours each.
Essential Skills
+ Bachelor's Degree in science, exercise science, kinesiology, or biology.
+ Technical proficiency in operating test devices and conducting data entry.
+ Ability to execute test protocols and direct participants through studies.
+ Familiarity with gym equipment and exercise knowledge.
+ Capability to stand for an entire shift.
Additional Skills & Qualifications
+ Experience in human subject research.
+ Data analysis skills.
+ Experience as a personal trainer.
Work Environment
The role operates in a flexible and dynamic work environment with both morning (7:30 AM - 3:00 PM) and evening (2:00 PM - 9:00 PM) shifts available. Candidates can work either or both shifts, with options for double shifts. Work involves standing for long periods, some desk work, and participant interaction in a simulated environment. Casual yet presentable attire is required, suitable for active demonstrations. Training is typically conducted during the day shift but accommodations can be made for evening shifts. The study may occasionally take place outdoors, and lunches are provided.
Job Type & Location
This is a Contract position based out of Tampa, Florida.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Tampa,FL.
Application Deadline
This position is anticipated to close on Sep 12, 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 Title: Study Coordinator
Job Description
Engage in human subject research, focusing on wearable devices in an exercise setting. Monitor participants, collect data, and ensure the proper setup and functioning of technology products throughout the study sessions. Facilitate participant interaction and data collection according to established protocols.
Responsibilities
+ Conduct research with human participants using wearable devices.
+ Consent participants, and take necessary vitals and measurements such as height, weight, and EKG throughout sessions.
+ Ensure participants are properly set up with devices and monitoring equipment.
+ Observe participants using devices during various activities according to protocol.
+ Ensure data monitoring and collection are functioning properly, both through equipment and manually.
+ Guide participants throughout the study sessions, which can last up to 2.5 hours each.
Essential Skills
+ Bachelor's Degree in science, exercise science, kinesiology, or biology.
+ Experience in research, data entry, and protocol implementation.
+ Technical proficiency in operating test devices and conducting data entry.
+ Ability to execute test protocols and direct participants through studies.
+ Familiarity with gym equipment and exercise knowledge.
+ Capability to stand for an entire shift.
Additional Skills & Qualifications
+ Experience in human subject research.
+ Data analysis skills.
+ Experience as a personal trainer.
Work Environment
The role operates in a flexible and dynamic work environment with both morning (7:30 AM - 3:00 PM) and evening (2:00 PM - 9:00 PM) shifts available. Candidates can work either or both shifts, with options for double shifts. Work involves standing for long periods, some desk work, and participant interaction in a simulated environment. Casual yet presentable attire is required, suitable for active demonstrations. Training is typically conducted during the day shift but accommodations can be made for evening shifts. The study may occasionally take place outdoors, and lunches are provided.
Job Type & Location
This is a Contract position based out of Tampa, Florida.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Tampa,FL.
Application Deadline
This position is anticipated to close on Sep 17, 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 Title: Study Coordinator
Job Description
We are seeking a dedicated Study Coordinator to conduct human subject research, focusing on wearable devices in an exercise setting. The role involves monitoring participants, collecting data, and ensuring the smooth operation of technology products throughout the study.
Responsibilities
+ Conduct research with human participants using wearable devices in an exercise setting.
+ Monitor and collect data throughout the study sessions, each lasting up to 2.5 hours.
+ Consent participants and take necessary vitals and measurements, such as height, weight, and EKG.
+ Ensure proper setup of devices and monitoring equipment for participants.
+ Observe participants using devices according to protocol and ensure data monitoring functions properly.
+ Collect data through equipment and manually, ensuring accuracy and completeness.
+ Guide participants throughout the study and provide necessary support.
Essential Skills
+ Experience in research and data entry.
+ Ability to implement study protocols.
+ Bachelor's degree in Science, Exercise Science, Kinesiology, or Biology.
+ Technical proficiency with test devices and data entry.
+ Ability to stand for an entire shift and familiarity with gym equipment.
Additional Skills & Qualifications
+ Experience in human subject research and data analysis.
+ Experience as a personal trainer.
Work Environment
The position offers flexible shifts, with options for AM (7:30 AM to 3:00 PM) or PM (2:00 PM to 9:00 PM) shifts, and the possibility of double shifts. Lunches are provided, and the role requires being on your feet for long periods, some desk work, and working with participants in a simulated environment. Dress code is casual but presentable. The study may include outdoor activities, and training is typically conducted during the day but can be accommodated for evening shifts if needed. The study will run through the end of the year, with potential continuation into early next year.
Job Type & Location
This is a Contract position based out of Natick, Massachusetts.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Natick,MA.
Application Deadline
This position is anticipated to close on Sep 17, 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 Title: Study Coordinator
Job Description
We are seeking a dedicated Study Coordinator to conduct human subject research, focusing on wearable devices in an exercise setting. The role involves monitoring participants, collecting data, and ensuring the smooth operation of technology products throughout the study.
Responsibilities
+ Conduct research with human participants using wearable devices in an exercise setting.
+ Monitor and collect data throughout the study sessions, each lasting up to 2.5 hours.
+ Consent participants and take necessary vitals and measurements, such as height, weight, and EKG.
+ Ensure proper setup of devices and monitoring equipment for participants.
+ Observe participants using devices according to protocol and ensure data monitoring functions properly.
+ Collect data through equipment and manually, ensuring accuracy and completeness.
+ Guide participants throughout the study and provide necessary support.
Essential Skills
+ Bachelor's degree in Science, Exercise Science, Kinesiology, or Biology.
+ Technical proficiency with test devices and data entry.
+ Ability to stand for an entire shift and familiarity with gym equipment.
Additional Skills & Qualifications
+ Experience in human subject research and data analysis.
+ Experience as a personal trainer.
Work Environment
The position offers flexible shifts, with options for AM (7:30 AM to 3:00 PM) or PM (2:00 PM to 9:00 PM) shifts, and the possibility of double shifts. Lunches are provided, and the role requires being on your feet for long periods, some desk work, and working with participants in a simulated environment. Dress code is casual but presentable. The study may include outdoor activities, and training is typically conducted during the day but can be accommodated for evening shifts if needed. The study will run through the end of the year, with potential continuation into early next year.
Job Type & Location
This is a Contract position based out of Natick, Massachusetts.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 Natick,MA.
Application Deadline
This position is anticipated to close on Sep 12, 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.

Title: Study Coordinator
Location: Rochester, NY (100% onsite)
Type: 3 month contract
Pay Rate: $25-28/hr.
Start Date: ASAP
Key Responsibilities
- Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study related supplies and equipment, assisting with monitoring visits, attending Investigator Meetings, and assisting with query resolution, as required.
- Provide the highest level of care and excellent customer service for study participants.
- Collaborate with lab staff to plan for and manage laboratory samples throughout the length of the study, including review of the laboratory manual.
- Ensure study drug is dispensed, accounted for and returned to the Sponsor per protocol.
- Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB (through Regulatory) within 24 hours of site being notified of event, including collecting all required information for initial and follow-up reporting.
- Ensure visit logs and CTMS visit status are accurate and complete.
- Facilitate ongoing Quality Assurance (QA) review of studies, in collaboration with the QA department, including assisting with risk assessments, root cause analysis, and development of corrective and preventative actions as applicable.
Qualifications
- Excellent verbal and written communication skills.
- Excellent interpersonal and customer service skills.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong analytical and problem-solving skills.
- Ability to prioritize tasks and to delegate them when appropriate.
- Ability to function well in a high-paced environment
Education and Experience
- 4-year degree in related field or NYS LPN License required, or related experience as a clinical trial coordinator.
- At least three years' experience in clinical research setting.
- CCRC preferred
Ref: #568-Clinical
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Job Title: Study Coordinator
Job Description
The Study Coordinator will conduct human subject research, focusing on wearable devices in an exercise setting. This role involves monitoring participants, collecting data, and ensuring the accuracy of data collection throughout each session.
Responsibilities
+ Conduct research with human participants using wearable technology in an exercise environment.
+ Monitor and collect data from participants, ensuring accurate data collection through both equipment and manual methods.
+ Guide participants through the study, ensuring they are properly set up with devices and monitoring equipment.
+ Obtain consent from participants and take necessary vitals and measurements (height, weight, EKG) at the start and end of each session.
+ Observe participants using devices during various activities, following the protocol.
+ Ensure proper functioning of data monitoring systems throughout the study sessions.
Essential Skills
+ Bachelor's degree in science, exercise science, kinesiology, or biology.
+ Technical proficiency to operate test devices and perform data entry.
+ Capability to direct participants through studies, with examples of patient care or people interaction.
+ Familiarity with gym equipment and knowledge of exercise.
Additional Skills & Qualifications
+ Ability to stand for an entire shift.
+ Experience in clinical research.
+ Experience in human subject research and data analysis.
+ Experience as a personal trainer.
Work Environment
The role involves working 12-hour days, from 7:00 am to 7:00 pm, two days a week. The coordinator will work directly with participants in a simulated environment, occasionally performing outdoor studies. The dress code is casual, suitable for active participation while maintaining a presentable appearance. The position offers flexibility in scheduling, ideal for graduate students seeking experience in clinical research. The coordinator will be on their feet for extended periods, with some desk work involved.
Job Type & Location
This is a Contract position based out of New York, New York.
Pay and Benefits
The pay range for this position is $25.00 - $25.00/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 York,NY.
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.

Title: Study Coordinator
Location: Buffalo, NY (100% onsite)
Type: 3 month contract
Pay Rate: $25-28/hr.
Start Date: ASAP
Key Responsibilities
- Manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study related supplies and equipment, assisting with monitoring visits, attending Investigator Meetings, and assisting with query resolution, as required.
- Provide the highest level of care and excellent customer service for study participants.
- Collaborate with lab staff to plan for and manage laboratory samples throughout the length of the study, including review of the laboratory manual.
- Ensure study drug is dispensed, accounted for and returned to the Sponsor per protocol.
- Ensure Serious Adverse Events (SAE's) are reported to Principal Investigator, Sponsor, and IRB (through Regulatory) within 24 hours of site being notified of event, including collecting all required information for initial and follow-up reporting.
- Ensure visit logs and CTMS visit status are accurate and complete.
- Facilitate ongoing Quality Assurance (QA) review of studies, in collaboration with the QA department, including assisting with risk assessments, root cause analysis, and development of corrective and preventative actions as applicable.
Qualifications
- Excellent verbal and written communication skills.
- Excellent interpersonal and customer service skills.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong analytical and problem-solving skills.
- Ability to prioritize tasks and to delegate them when appropriate.
- Ability to function well in a high-paced environment
Education and Experience
- 4-year degree in related field or NYS LPN License required, or related experience as a clinical trial coordinator.
- At least three years' experience in clinical research setting.
- CCRC preferred
Ref: #568-Clinical
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

**Why People choose to work at Labcorp:**
At Labcorp, it is our people that make us great - it's what our clients, our partners and, most importantly, what our employees say. Here, you will have the opportunity to collaborate with extraordinary people with diverse viewpoints. You will discover your own outstanding potential as we build an even stronger organization with industry leaders from early development to the clinic and beyond. We help our clients develop medicines that improve health and improve lives of their family and friends.
**We have an exciting opportunity for a Study Coordinator for Preclinical (Animal) Research Studies in Madison, WI.**
**Position Summary:**
The Study Coordinator is responsible for coordinating the activities of routine and non-routine studies, in compliance with the appropriate company standards, GLP and regulatory guidelines in a timely, efficient manner. General assistance to Study Directors will be an essential part of the role and additional non-study specific support may be given to key clients. Additional daily duties may include support of other functions within Safety Assessment.
**Essential Duties:**
+ Provides administrative and scientific support for toxicology studies, including pre-study tasks (e.g., protocol development, costing, scheduling), monitoring the in-life progress of assigned studies, and interacting with clients.
+ Provides administrative backup support for Study Directors on day-to-day study-specific activities or tasks.
+ Learns to ensure study compliance with the protocol, standard operating procedures, Good Laboratory Practices, and other regulatory guidelines.
+ Learns to plan, prioritize, and manage a workload and the associated responsibilities.
+ Serves as a contact, along with the Study Director, in communication and interactions with other departments and clients, with assistance as applicable.
+ Learns to compile data for clients for regular study progress updates.
+ Learns to draft protocols and amendments for Study Director Review and approval.
+ Ensures all client comments on protocols and amendments are addressed in a timely manner.
+ Schedules and participates in pre-initiation and other study-related meetings, as required, and takes and distributes pre-initiation meeting minutes.
+ Learns to address and review quality assurance audits relating to protocols and amendments and reports (as applicable), with oversight. Follows up with appropriate personnel to ensure all necessary document/data clarifications are completed in the specified timelines.
+ Prepare shipping documentation including CITES application requests and any other associated shipping documentation, as required per study
**Education/Experience:**
+ Bachelor's degree in a related science field
+ 2 years of previous related job experience
+ Strong knowledge of office software (e.g., Microsoft® Office, especially Word and Excel)
**Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here ( .
**Labcorp is proud to be an Equal Opportunity Employer:**
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
**We encourage all to apply**
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site ( or contact us at Labcorp Accessibility. ( ) For more information about how we collect and store your personal data, please see our Privacy Statement ( .