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Research Study Coordinator Jobs in Raleigh, NC (NOW HIRING)

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Retirement

  • PTO

The study is taking place at four sites-Durham and Orange Counties, NC; Portland, ME; Miami, FL ... The hired candidate will work with the Lead Coordinator and PI to identify when research-related ...

Responsibilities include participant recruitment and screening, coordinating focus groups ... study questionnaires through REDCap, maintaining study records, and assisting with data management.

Research Technician

Raleigh, NC

$17.50 - $24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... study coordination. * Perform pain assessments and provide patient care support for clinical and laboratory research subjects. * Collect, process, and analyze kinetic, behavioral, and laboratory ...

Research Technician

Raleigh, NC · On-site

$49K - $57K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... study coordination. * Perform pain assessments and provide patient care support for clinical and laboratory research subjects. * Collect, process, and analyze kinetic, behavioral, and laboratory ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Retirement

  • PTO

CLINICAL RESEARCH COORDINATOR Duke Vaccine and Trials Unit - Duke Human Vaccine Institute Be You ... May train others. Prepares for and provides support for study monitoring and audit visits ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Retirement

  • PTO

CLINICAL RESEARCH COORDINATOR Duke Vaccine and Trials Unit - Duke Human Vaccine Institute Be You ... May train others. Prepares for and provides support for study monitoring and audit visits ...

Serbanescu), the study coordinator, research staff, and collaborating physician-scientists to support MICRO-ICU and related translational studies. Primary responsibilities will include: Screening ICU ...

Serbanescu), the study coordinator, research staff, and collaborating physician-scientists to support MICRO-ICU and related translational studies. Primary responsibilities will include: • Screening ...

Clinical Study Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ... At least eight years of clinical research experience, including at least two years of experience in ...

Clinical Study Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ... At least eight years of clinical research experience, including at least two years of experience in ...

Clinical Study Manager

Durham, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ... At least eight years of clinical research experience, including at least two years of experience in ...

Showing results 41-60

Research Study Coordinator information

See Raleigh, NC salary details

$20.9K

$78.3K

$109.4K

How much do research study coordinator jobs pay per year?

As of Aug 19, 2026, the average yearly pay for research study coordinator in Raleigh, NC is $78,321.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,300.00 and $96,700.00 per year, depending on experience, location, and employer.

What is a research study coordinator?

Research Study Coordinators are professionals responsible for managing and overseeing the day-to-day operations of clinical trials or research studies. They ensure that studies are conducted according to protocols, regulatory guidelines, and ethical standards. Their duties often include recruiting and enrolling participants, collecting and managing data, coordinating with research teams, and maintaining accurate documentation. Research Study Coordinators play a crucial role in ensuring the integrity and success of research projects.

What are the key skills and qualifications needed to thrive as a research study coordinator?

To thrive as a Research Study Coordinator, you need a background in life sciences or health-related fields, experience with research protocols, and often a bachelor's or master's degree. Familiarity with data management systems, regulatory compliance platforms (such as IRB software), and sometimes certifications like CCRC are typically required. Strong organizational abilities, attention to detail, and effective communication help manage study logistics and participant interactions. These skills are important to ensure studies run efficiently, data is accurate, and compliance with ethical and regulatory standards is maintained.

What are some typical challenges faced by research study coordinators when managing multiple clinical trials simultaneously?

Research Study Coordinators often juggle several studies at once, which requires exceptional organizational and time-management skills. Common challenges include keeping meticulous records for each trial, ensuring protocol compliance, and coordinating schedules among investigators, sponsors, and participants. Managing regulatory documentation and staying updated with changing study protocols can also be demanding. Successful coordinators proactively communicate with their teams and utilize digital tools to streamline processes, ensuring each study stays on track.

What is the difference between Research Study Coordinator vs Research Assistant?

AspectResearch Study CoordinatorResearch Assistant
CredentialsBachelor's degree often required; certification optionalTypically requires a bachelor's degree or current student status
Work EnvironmentLeads study activities, manages protocols, interacts with staff and participantsSupports data collection, performs administrative tasks, assists with experiments
Employer & Industry UsageUsed in clinical research, academic, and healthcare settingsCommon in research labs, universities, and clinical trials

The Research Study Coordinator and Research Assistant roles often overlap in credentials and work environments, but coordinators typically have more responsibility in managing study protocols and participant interactions. Both roles are essential in research settings, with coordinators taking a leadership role in study execution.

What job categories do people searching Research Study Coordinator jobs in Raleigh, NC look for?

The top searched job categories for Research Study Coordinator jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Research Study Coordinator jobs?

Cities near Raleigh, NC with the most Research Study Coordinator job openings:

Infographic showing various Research Study Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 12% Part Time, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $78,321 per year, or $37.7 per hour.

Clinical Research Coordinator

Duke University

Durham, NC • On-site

$23.50 - $31.25/hr

Contractor

Medical, Dental, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Duke University rating

6.7

Company rating: 6.7 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

487th of 619 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.
About the Bellwether Collaborative for Health Justice:
As part of the Duke University Department of Population Health Sciences, it is the mission of the Bellwether Collaborative for Health Justice to shine a light on how the criminal legal system acts a structural determinant of health and impacts population and individual level health outcomes. We are an interdisciplinary research team, led by Dr. Lauren Brinkley-Rubinstein. Our work draws on the expertise of criminal legal system-involved persons and carceral and community stakeholders to inform innovative research that has practice and policy implications.
About the Research:
Overdose is one of the leading causes of death in the US. People who are exposed to or impacted by the criminal legal system disproportionately report using substances and experience high rates of overdose. Community Paramedic or Post-Overdose Response Team programs have grown across the country to address this crisis.
These teams respond during and after overdoses to offer life-saving support-including naloxone, medications for opioid use disorder (MOUD), and connections to health and social services, to help people get care rather than face arrest or incarceration. However, these programs mostly focus on individual-level care. Research shows that broader issues-like lack of housing, difficulty accessing public benefits, and unmet legal needs-also drive overdose risk. These are sometimes called "health-harming legal needs" (HHLN). Medical-Legal Partnerships bring together legal and healthcare professionals to address these deeper challenges and reduce the chance of future overdose harm.
The hired candidate will join our work on the CROSSROADS study, which is an Implementation Effectiveness Trial designed to compare the community paramedic standard of care to an intervention that leverages Medical-Legal Partnerships. The study is taking place at four sites-Durham and Orange Counties, NC; Portland, ME; Miami, FL; and Pittsburgh, PA. The hired position will join an existing team to co-lead research activities at the NC site, ensure timely completion of all regulatory activities, and provide administrative support to the academic partners at Brown University, the University of Miami, Boston Medical Center, and University of Pittsburgh.
Minimum Requirements:
An Associate's degree is required.
Work requires a minimum of two years of research experience.
Special Skills:
  • Previous experience supporting the work of multi-site or complex research studies;
  • Experience or expressed interest in working with individuals impacted by the criminal legal system;
  • Interest and experience in scholarly writing.

Requested Application Materials:
Please provide a resume/CV, references, and a cover letter with your application. In your cover letter, please address any research experience you have, your interest/experience in working with populations affected by incarceration, and any experience/interest you have working with individuals impacted by OUD or the criminal legal system.
Must live in the Durham/Orange County area.
Be Bold.
About the Position:
The Bellwether Collaborative for Health Justice seeks a Clinical Research Coordinator to co-lead all aspects of the CROSSROADS Study in Durham and Orange County, North Carolina. The responsibilities of this position include the following:
Research Operations:
  • Establishing Agreements: The hired candidate will work with the Lead Coordinator and PI to identify when research-related agreements are required for their project (examples: independent contractor agreements, data use agreements, sub-award contracts, etc.).
  • Regulatory Knowledge: The hired candidate will have a working knowledge of regulatory and institutional policies (examples: IRB submission, required enrollment reporting, etc.) and ensure team-wide compliance and adherence to required policies.
  • Regulatory Oversight: The hired candidate will prepare the study site for monitoring and audit visits. They will also work with the study team to address and correct any concerns identified by reviewers.
  • Participant-Level Documentation: The hired candidate will be responsible for maintaining participant-level documentation, tracking study enrollment and retention, and developing and implementing strategies to create high levels of participant engagement.
  • Screening and Enrollment: The hired candidate will be responsible for screening participants for eligibility and enrollment. They will create study-level documentation and SOPs. They will also provide enrollment training and resources for study staff across all study sites.
  • Participant Study Visits: The hired candidate will be responsible for the preparation and administration of study visits. They will create study-level documentation and training materials to ensure consistency among staff across all participating sites.
  • Leading Meetings: The hired candidate will take a leadership role in managing project meetings for the Duke site as well as larger, cross-site meetings. They will work closely with project leadership to facilitate team meetings, including identifying priorities, preparing and distributing agendas, and creating and distributing meeting minutes.

Research Ethics
  • Adverse Events: The hired candidate will monitor study activities for adverse events and ensure timely reporting to the Lead Coordinator, PI, and required parties.
  • Participant Consent and Documentation: The hired candidate will develop participant consent materials in close consultation with the Duke research team. They will also be responsible for developing SOPs and training staff on adequate consent processes and documentation.
  • IRB submission: The hired candidate will be responsible for developing and submitting IRB protocols.
  • Regulatory and Safety Reporting: The hired candidate will prepare and submit regulatory and safety documentation to sponsors and other agencies.

Data Management
  • Data Entry: The hired candidate will collect and maintain study data.
  • SOP Development: The hired candidate will develop data management workflows and SOPs for their study.
  • Supervision: The hired candidate will train research staff in data collection protocols and provide regular oversight over data quality and completeness. They will ensure that all members of the study team adhere to data security protocols and will identify and escalate data management issues appropriately.
  • Quality Assurance: The hired candidate will provide routine data oversight and quality checks to ensure consistency with study protocols and federal and institutional requirements.

Scientific Contributions
  • Grant Writing: The hired candidate will contribute meaningfully to the development of grant submissions and funding opportunities.
  • Protocol Development: The hired candidate will work closely with the PI to develop research protocols consistent with best research practices.
  • Scholarly Product Development: The hired candidate will contribute to the development of scholarly products, including leading presentations, creating academic posters, serving as an author on manuscripts, etc. The hired candidate will also contribute to the distribution of study findings to non-scientific audiences (example: blog posts, white papers, stakeholders, etc.)

Study and Site Management
  • Research Activity Management: The hired candidate will use Duke clinical research management systems, like Oncore, to track and manage participant activities, such as enrollment, participant payment, interviews, appointments, etc.
  • Participant Enrollment Reporting: The hired candidate will use Duke clinical research management systems, like Oncore, to track and report participant enrollment data, maintain research protocols, and track all research activities.
  • Equipment and Supply Management: The hired candidate will be responsible for maintaining research materials, supplies, and equipment.

Leadership:
  • Professional Development: The hired candidate will have significant opportunity for professional development. They will work closely with their supervisor and PI to identify and facilitate training opportunities for themselves and other members of the study team.
  • Continuing Education: The hired candidate will stay up-to-date with research best practices by attending talks, trainings, and workshops. They will also identify opportunities for members of their team to gain content expertise.
  • Scientific-Community Engagement: The hired candidate will serve as a representative for the research team. They may also participate in committees or workgroups to disseminate study findings and research best practices.
  • Interpersonal Skills: The hired candidate will build successful, respectful, collaborative relationships with participants, community partners, and institutional stakeholders (e.g., community-based organizations, healthcare providers, and criminal legal system partners), using culturally responsive and trauma-informed approaches.
  • Conflict Management: The hired candidate will recognize, navigate, and respond to interpersonal or organizational challenges with professionalism and sound judgment. They will address concerns directly when appropriate and escalate issues through appropriate channels as needed.

Choose Duke.
Join our award-winning team as identified by Forbes magazine as America's Best Large Employer 2024 and be part of an inclusive culture that values excellence, innovation, and discovery. As an organization, we have exciting opportunities to be forward-thinking leaders in our field. We want talented individuals to join us, examine our current operations, and create innovative solutions that will revolutionize and enhance the way we approach our work.
Duke University is consistently ranked among the top universities worldwide and is renowned for its cutting-edge research across disciplines.
Beyond the engaging work, you'll also benefit from Duke's competitive benefits package including health insurance plans, generous paid time off, retirement programs with employer contributions, tuition assistance for employees and their children, and more.
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $59,829.00 to USD $99,960.00. 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.

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Colleges, universities, and professional schools and hospitals

Company size

10,000+ Employees

Headquarters location

Durham, NC, US