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Study Coordinator Jobs in Raleigh, NC (NOW HIRING)

Fortrea

Project Coordinator I, PC Academy

Durham, NC · Remote

$28 - $35/hr

As a Project Coordinator, you'll play a critical role in keeping studies organized, on track, and audit-ready-working alongside experienced project managers and cross-functional teams in a fast-paced ...

Duke University

POSTDOCTORAL ASSOCIATE

Durham, NC

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

Duke University

POSTDOCTORAL ASSOCIATE

Durham, NC · On-site

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

Actalent

Clinical Trial Manager- Hybrid

Raleigh, NC · Hybrid

Contract Clinical Study Manager Hybrid Raleigh-Durham (RTP) The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies from start ...

Actalent

Clinical Trial Manager- Hybrid

Cary, NC · Hybrid

Contract Clinical Study Manager Hybrid Raleigh-Durham (RTP) The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies from start ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

Clinical Research Coordinator (CRC) - Raleigh, NC Location: Raleigh, NC Work Setup: On-site ... Perform study-related clinical procedures, including ECGs, vital signs, specimen collection, and ...

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Study Coordinator information

See Raleigh, NC salary details

$21.4K

$53.3K

$78.2K

How much do study coordinator jobs pay per year?

As of Aug 14, 2026, the average yearly pay for study coordinator in Raleigh, NC is $53,319.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,800.00 and $60,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What is a study coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

What are some common challenges study coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

More about Study Coordinator jobs

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

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

What are popular job titles related to Study Coordinator jobs in Raleigh, NC?

For Study Coordinator jobs in Raleigh, NC, the most frequently searched job titles are:

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

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

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

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

Study Coordinator jobs near you
Infographic showing various Study Coordinator job openings in Raleigh, NC as of July 2026, with employment types broken down into 70% Full Time, 10% Part Time, and 20% Contract. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $53,319 per year, or $25.6 per hour.

Clinic Nurse (RN)

Careers Integrated Resources Inc

Chapel Hill, NC • On-site

Other

Posted 3 days ago

New

Job description

Research Study Coordinator

Must have: Ability to maintain a high level of detail and accuracy in work Demonstrated ability to communicate effectively and respectfully with individuals of diverse backgrounds Excellent computer skills IV Care Must have comfortability working and interacting with all levels of University employees. Looking for high-level customer service and computer skills, proactive (always looking for ways to contribute to the team), and a team player. Proficient with inserting PIV catheter's Standardized Procedures

Job Description: Pay is ***/hr.

UNC Gillings School of Global Public Health, Department of Nutrition is implementing two exciting research studies--the All of Us Research Program and the first All of Us ancillary study, Nutrition for Precision Health (NPH). All of Us is a unique research program funded by the NIH to build one of the most diverse health databases in history to recruit at least one million participants nationwide. A subset of All of Us participants will also be recruited into Nutrition for Precision Health, powered by the All of Us Research Program with the study goal of developing algorithms that predict individual responses to food and dietary patterns. The UNC Clinical Center (UNC-CC) is one of six clinical centers across the country that will recruit a diverse cohort of adults from rural and urban communities and implement the All of Us and NPH study protocols to study variability in physiologic responses to diet. Join our team as we work on these innovative studies.

Working in coordination with onsite research staff, this person will be responsible for a variety of duties including management of liquid and regular meal tolerance tests and assessment of participant safety. Specific duties are included below but may vary depending on the needs of the study.

  • Placement and accessing of IVs to allow for repeated blood collection.
  • Clinical review and participant communication regarding safety assessments (eligibility and adverse events)
  • Perform venipuncture as needed
  • Follow detailed study protocol and collect the nine timed samples via IV within a 3-5 minute window of the time
  • Client Data collection including providing reminders and instructions to study participants according to the study protocol
  • Assist with other study activities to ensure the successful completion of the study aims

Requirements:

-Must be licensed as an RN, LPN, or AEMT in the state of North Carolina. Preferred: -At least 6 months of previous experience with IV insertion and drawing blood.

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