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Clinical Trial Associate Jobs in Raleigh, NC (NOW HIRING)

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH ... Ensure copies/originals (as required) site documents are available for filing in the Trial Master ...

We are currently seeking a Lead Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial ...

Lafata Lab Postdoctoral Associate Be You. At Duke, we believe groundbreaking discoveries happen ... Support large-scale clinical trial operations through rigorous data management practices. * Foster ...

Lafata Lab Postdoctoral Associate Be You. At Duke, we believe groundbreaking discoveries happen ... Support large-scale clinical trial operations through rigorous data management practices. * Foster ...

Support and maintain clinical project documents in paper and/or electronic Trial Master Files and ... Research Associates (RAs) in clinical projects * Assist with orientating new Clinical staff

We translate unique clinical, medical affairs and commercial insights into outcomes to address ... Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician ...

We translate unique clinical, medical affairs and commercial insights into outcomes to address ... Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician ...

Showing results 41-60

Clinical Trial Associate information

See Raleigh, NC salary details

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$38

$68

How much do clinical trial associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for clinical trial associate in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.

What is a clinical trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

What are the key skills and qualifications needed to thrive as a clinical trial associate?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

What is the difference between Clinical Trial Associate vs Clinical Research Coordinator?

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Trial jobs in Raleigh, NC?

The most popular types of Clinical Trial jobs in Raleigh, NC are:

What are popular job titles related to Clinical Trial Associate jobs in Raleigh, NC?

For Clinical Trial Associate jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Clinical Trial Associate jobs?

Cities near Raleigh, NC with the most Clinical Trial Associate job openings:

Infographic showing various Clinical Trial Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $80,843 per year, or $38.9 per hour.

Clinical Research Nurse Coordinator - Duke Cancer Institute

Duke University

Durham, NC • On-site

$66K - $83K/yr

Full-time

Medical, Dental, Retirement

Re-posted 10 days ago


Duke University rating

6.7

Company rating: 6.7 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

491st of 627 rated colleges and universities


Job description

School of Medicine:
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.
Be You.
The Duke Cancer Institute (DCI) is seeking a Clinical Research Nurse Coordinator to join our GU (Genitourinary) Clinical Research Program. In this role, you will provide leadership and hands-on coordination for multiple, complex oncology clinical trials, including studies involving Investigational Products (IP). You will play a critical role in advancing cancer research by supporting participants throughout the research process while ensuring studies are conducted safely, ethically, and in full compliance with regulatory and institutional requirements.
You will work closely with Principal Investigators, sponsors, study teams, and the Oncology Clinical Research Unit (CRU) to bring innovative therapies to patients. This role blends direct patient care, clinical research operations, and collaborative leadership, making it ideal for a nurse who is passionate about oncology research, patient advocacy, and continuous learning.
Minimum Requirements
  • Graduation from an accredited BSN, Associate Degree in Nursing, or Nursing Diploma program
  • Current or compact Registered Nurse (RN) licensure in the state of North Carolina
  • BLS certification
  • Minimum of 12 months of clinical nursing experience
  • Ability to maintain compliance with Duke, hospital, and unit-specific training and competency requirements
  • Active RN status with the North Carolina Board of Nursing (NCBON)

Preferred Qualifications
  • At least two (2) years of patient-facing clinical research or direct patient care experience
  • Experience with clinical trial activities such as screening, consenting, protocol implementation, and research involving human participants
  • Experience working with oncology patient populations
  • Strong organizational skills with the ability to manage multiple, complex clinical trials simultaneously
  • Experience using electronic health records (EHR), Electronic Data Capture (EDC) systems, and/or Clinical Trial Management Systems (CTMS)
  • Excellent written and verbal communication skills

Be Bold.
In this role, you will coordinate, manage, and lead all aspects of assigned oncology clinical trials, ensuring high-quality execution and participant-centered care.
  • Coordinate clinical trial operations and site management, including feasibility assessments, participant recruitment and retention strategies, and study start-up and closeout activities
  • Recruit, screen, consent, enroll, schedule, and conduct study visits in collaboration with Principal Investigators and study teams; document all study activities accurately and in compliance with protocol requirements
  • Ensure regulatory and institutional compliance by maintaining regulatory binders, enrollment logs, delegation of authority logs, adverse event documentation, and required submissions
  • Serve as the primary liaison between sponsors, monitors, investigators, and internal study personnel; communicate proactively and escalate issues appropriately
  • Manage study data and documentation, including accurate and timely EDC entry; identify and resolve data discrepancies while ensuring data security and integrity
  • Monitor study finances, including participant care costs, study payments, budget development support, and financial milestone tracking
  • Provide leadership and mentorship within the research team; serve as an expert resource and support training and professional development of colleagues
  • Promote ethical research conduct by clearly distinguishing clinical care from research activities for participants and staff, reinforcing informed consent principles and regulatory standards
  • Deliver direct RN clinical care in the research setting, including medication administration, chemotherapy administration, patient assessments, adverse event recognition, patient education, and collaboration with the interdisciplinary medical team

Choose Duke.
The Duke Cancer Institute is a nationally recognized leader in cancer research, treatment, and prevention. By joining the GU Clinical Research Program, you will contribute to cutting-edge oncology trials that directly impact patient outcomes and advance scientific discovery.
At Duke, you'll find a collaborative, mission-driven environment that values excellence, integrity, and compassion. You'll have access to robust professional development opportunities, participation in scientific presentations and publications, and the support of a highly engaged multidisciplinary team.
Job Code: 00001203 CLINICAL RESEARCH NURSE COORDINATOR
Job Level: 54
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $64,966.00 to USD $104,996.00. 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:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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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