Associate's degree in Clinical Research or successful completion of the approved Clinical Research ... Ability to perform study-related administrative and operational tasks * Some roles may involve ...
Associate's degree in Clinical Research or successful completion of the approved Clinical Research ... Ability to perform study-related administrative and operational tasks * Some roles may involve ...
Clinical Research Associate 3
$50.02 - $62.53/hr
Clinical Research Associate 3 Pay Rate: $50.02 - $62.53/hr. Location: Durham, NC ZIP Code: 27701 ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
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Clinical Research Associate 3
$50.02 - $62.53/hr
Clinical Research Associate 3 Pay Rate: $50.02 - $62.53/hr. Location: Durham, NC ZIP Code: 27701 ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
Clinical Research Associate 3 Duration: 12+ Months Location: Durham, NC The Clinical Research ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
Quick apply
Clinical Research Associate 3 Duration: 12+ Months Location: Durham, NC The Clinical Research ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Assess and review the regulatory ...
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Assess and review the regulatory ...
Assoc Site Activation Manager
Durham, NC · On-site
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Assess and review the regulatory ...
Assoc Site Activation Manager
Durham, NC · On-site
Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Assess and review the regulatory ...
Sr. Clinical Operations Lead (Clinical Trial Manager)
Raleigh, NC · Remote
$86K - $143K/yr
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...
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Sr. Clinical Operations Lead (Clinical Trial Manager)
Raleigh, NC · Remote
$86K - $143K/yr
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...
Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and ... The COL will develop study tools for site and CRA use, review visit reports, review and track ...
Clinical Research Associate 3
Durham, NC · On-site
$50 - $62/hr
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
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Clinical Research Associate 3
Durham, NC · On-site
$50 - $62/hr
The Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative ... Experience monitoring National Cancer Institute (NCI) studies, cooperative group studies, or other ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Clinical Research Coordinator
$23.50 - $31.25/hr
Studies will focus on neurocognition and health disparities, with a focus in the Hispanic/Latino ... Completion of an Associate's degree Experience: Work requires a minimum of two years of relevant ...
Clinical Research Coordinator
$23.50 - $31.25/hr
Studies will focus on neurocognition and health disparities, with a focus in the Hispanic/Latino ... Completion of an Associate's degree Experience: Work requires a minimum of two years of relevant ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
... clinical studies, stability studies, ETPs, and Regulatory submissions. Primary responsibilities for QA III role: * Develops alternative solutions to problems, handles complex problems independently.
... clinical studies, stability studies, ETPs, and Regulatory submissions. Primary responsibilities for QA III role: * Develops alternative solutions to problems, handles complex problems independently.
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Quick apply
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...
Clinical Research Associate II/III - US
Durham, NC · On-site +1
We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence. With operations in ...
Clinical Research Associate II/III - US
Durham, NC · On-site +1
We specialise in Phase I-IV clinical studies, delivering Full-Service and Functional Service Provision (FSP) solutions that help sponsors move faster and execute with confidence. With operations in ...
Clinical Study Associate information
See Raleigh, NC salary details
$12.38 - $16.14
3% of jobs
$16.14 - $19.90
18% of jobs
$20.65 is the 25th percentile. Wages below this are outliers.
$19.90 - $23.66
20% of jobs
The median wage is $25.95 / hr.
$23.66 - $27.42
15% of jobs
$27.42 - $31.18
11% of jobs
$31.18 - $34.94
4% of jobs
$38.14 is the 75th percentile. Wages above this are outliers.
$34.94 - $38.70
5% of jobs
$38.70 - $42.46
8% of jobs
$42.46 - $46.22
6% of jobs
$46.22 - $49.98
6% of jobs
$49.98 - $53.74
3% of jobs
$12
$30
$53
How much do clinical study associate jobs pay per hour?
What are Clinical Study Associates?
What is the difference between Clinical Study Associate vs Clinical Research Coordinator?
| Aspect | Clinical Study Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficial | Bachelor's degree in health sciences or related field; certifications like CCRP advantageous |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospitals, clinics, research centers |
| Job Focus | Monitoring clinical trials, ensuring protocol compliance, data accuracy | Managing daily trial activities, patient recruitment, data collection |
| Employer & Industry Usage | Commonly employed in pharma and CROs | Primarily in healthcare and academic research settings |
Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.
What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?
What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Other
Medical, Dental, Retirement
Posted 11 days ago
Duke University rating
6.7
Based on 55 frontline employees who took The Breakroom Quiz
442nd of 560 rated colleges and universities
Job description
Be You.
The Clinical Research Unit at Duke University is looking for a Clinical Research Apprentice to join our team. This is an exciting opportunity to launch your clinical research career through a full-time apprenticeship supported by Bloomberg Philanthropies. In this role, you will gain hands-on experience while learning directly from experienced Clinical Research Professionals and building foundational skills in clinical trials, participant engagement, data management, and research operations.
You will work alongside research teams supporting studies across a variety of clinical research domains while completing work-based learning experiences designed to increase your knowledge, confidence, and independence over time. This role is ideal for someone passionate about healthcare, research, and improving patient outcomes through clinical discovery.
Minimum Requirements:
- Associate's degree in Clinical Research or successful completion of the approved Clinical Research Pre-Apprenticeship program
- Completion of the Durham Technical Community College Clinical Trials Research Associate's Degree training is required as a pre-requisite of the apprenticeship
- Ability to use standard computing software and web-based applications, including Microsoft Office products
- Strong communication and organizational skills
- Ability to work collaboratively in a team-based environment
- Interest in clinical research and participant-centered care
Preferred Qualifications:
- Prior exposure to healthcare or clinical environments
- Familiarity with electronic health records (EHR) or research databases
- Demonstrated attention to detail and ability to follow standard operating procedures
- Interest in learning Good Clinical Practice (GCP) and regulatory requirements
Other Requirements:
- Ability to attend departmental training sessions and professional development opportunities
- Ability to perform study-related administrative and operational tasks
- Some roles may involve specimen handling and management of research supplies
This position is:
- Onsite. The work is performed on-site or at a designated assignment location.
Be Bold.
In this role, you will:
- Perform clinical research tasks under supervision while increasing independence over time
- Assist with study participant screening, recruitment, scheduling, and study visit preparation
- Collect, document, and maintain participant and study-level information in compliance with protocols and SOPs
- Support specimen handling, inventory management, and investigational product accountability
- Enter and review research data for accuracy, completeness, and quality assurance
- Assist with informed consent documentation and participant communication
- Participate in study team meetings, monitoring visits, and audit preparation activities
- Learn and apply Good Clinical Practice (GCP), research ethics, and participant safety standards
- Collaborate with mentors and research professionals to develop clinical research competencies
and apply Good Clinical Practice (GCP), research ethics, and participant safety standards
Choose Duke.
At Duke University, you will join a collaborative research environment dedicated to advancing healthcare and scientific discovery. Through mentorship, hands-on learning, and structured professional development, you will gain valuable skills that prepare you for long-term success in clinical research.
Duke is committed to creating a community built on collaboration, innovation, creativity, and belonging. We value diverse perspectives and foster an environment where every team member feels respected, supported, and empowered to contribute.
Duke University is an Equal Opportunity Employer committed to providing employment opportunity without regard to age, color, disability, gender, gender identity or expression, genetic information, national origin, race, religion, sexual orientation, pregnancy-related conditions, or military status.
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $20.76 to USD $31.44. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.
Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/
Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status.
Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.
Essential Physical Job Functions:
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About Duke University
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Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate, and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries.
Industry
Colleges, universities, and professional schools and hospitals
Company size
10,000+ Employees
Headquarters location
Durham, NC, US