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Full Time Clinical Research Jobs in Raleigh, NC (NOW HIRING)

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

New

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

New

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

New

Care Access

Clinical Research Coordinator I

Raleigh, NC · On-site

$55K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

How This Role Makes a Difference The Clinical Research Coordinator's primary responsibilities are ... Benefits & Perks (US Full Time Employees) * Paid Time Off (PTO) and Company Paid Holidays * 100 ...

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Showing results 1-20

All JobsClinical Research JobsFull Time Clinical Research JobsFull Time Clinical Research Jobs in Raleigh, NC

Full Time Clinical Research information

See Raleigh, NC salary details

$47.6K

$104.3K

$183.7K

How much do full time clinical research jobs pay per year?

As of Aug 13, 2026, the average yearly pay for full time clinical research in Raleigh, NC is $104,339.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,700.00 and $119,100.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Clinical Research vs Clinical Research Coordinator?

AspectFull Time Clinical ResearchClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialTypically requires a bachelor's degree; certifications like CCRP or CRC advantageous
Work EnvironmentPharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Job ResponsibilitiesOversees entire clinical trials, manages teams, ensures complianceCoordinates daily trial activities, enrolls patients, collects data
Industry UsageCommonly employed in clinical research organizations and pharmaPrimarily found in research sites and hospitals

Full Time Clinical Research roles typically involve overseeing entire clinical trials and managing teams, often within pharmaceutical companies or CROs. Clinical Research Coordinators focus on daily trial operations at research sites, working closely with patients and data collection. Both roles require similar credentials and certifications, but differ mainly in scope and work environment.

What are the most commonly searched types of Clinical Research jobs in Raleigh, NC? The most popular types of Clinical Research jobs in Raleigh, NC are:
Full Time Clinical Research jobs near you
Infographic showing various Full Time Clinical Research job openings in Raleigh, NC as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 83% In-person, 4% Hybrid, and 13% Remote job distribution, with an average salary of $104,339 per year, or $50.2 per hour.

Clinical Research Coordinator

Revival Research Institute, LLC

Cary, NC • On-site

$23.75 - $31.75/hr

Full-time

Re-posted 22 days ago

Job description

Unique opportunity to make an Impact in the healthcare industry… 

Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since. Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Arizona. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials.  

As Revival Research Institute is growing, we are looking to add more qualified professionals to our team, who are looking for an opportunity to grow and learn with us.  

We are seeking a full-time Clinical Research Coordinator with a minimum of 2 year of clinical experience, for our Woman's Health site.  Someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow. However, this interest and background is not necessary, as our ideal candidate is an individual who is detail orientated, being able to maintain organized records, as well as someone who is motivated to learn new things, as our company is always growing and expanding into new therapeutic areas. We are looking for individuals that want the opportunity to learn and grow with us.  

Clinical Research Coordinators here at Revival Research Institute, should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. They are also responsible for assisting the Investigators along with other clinical staff, with any study related tasks as follows but not limited to: 

  1. Participates in research participant screening, recruitment and enrollment. Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight. Responsible for collecting, processing and shipping of research specimens, where applicable. 

  2. Documents study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits. Obtain, review and maintain source documents. 

  3. Maintains organization of all trial related documents and correspondence. Implement quality control and assurance methods. 

  4. Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting. 

  5. Maintain professional and technical knowledge about Clinical trials. 

  6. Research participant/family communication, protect patient confidentiality. 

Preferred Qualifications: 

  1. Education/ Training: Bachelor's degree in health-related field with one to two years relevant clinical experience OR Master's degree in medical related field with no research experience. Individuals with more experience are preferred, if qualifications exceed entry level, higher positions available. 

  2.  Phlebotomy skills preferred. 

  3. Certifications, Licensures, and Registrations: National Certification (CRA or ACRP), BLS Certification.  

  4. Additional Qualifications: Expert database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Maintain data integrity within the department. Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices. 

IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!! 

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