Clinical Research Jobs in South Carolina
Clinical research jobs in South Carolina are concentrated in academic medical centers, pharmaceutical contract research, and hospital-based trial units, with demand at every level from entry-level coordinators to principal investigators. The largest hiring activity is in Charleston, Columbia, and Greenville, where institutions like MUSC Health, Prisma Health, and Greenville Health System anchor a steady pipeline of openings. The most in-demand specialties are oncology trials, cardiovascular studies, and regulatory affairs coordination. Scan the live roles below and apply to whichever ones fit.
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Overview
Join our dynamic clinical research team as a Clinical Research Coordinator, where you'll play a pivotal role in advancing healthcare through meticulous management of clinical trials. This exciting position offers the opportunity to oversee research projects from inception to completion, ensuring compliance with regulatory standards and ethical guidelines. As a key team member, you'll coordinate study activities, monitor patient progress, and uphold the highest standards of data integrity and quality assurance. Bring your passion for research and healthcare to make a meaningful impact on patient outcomes and medical innovation.
Duties
- Coordinate and manage all aspects of clinical trials, including participant recruitment, scheduling, and follow-up.
- Ensure adherence to FDA regulations, ICH GCP guidelines, and healthcare compliance standards throughout the research process.
- Review and verify study documentation, including consent forms, case report forms, and regulatory submissions for accuracy and completeness.
- Monitor patient safety by tracking vital signs, blood sampling procedures, and adverse event reporting in accordance with clinical ethical guidelines.
- Utilize EMR (Electronic Medical Records) systems for data collection, entry, and management while maintaining strict confidentiality under HIPAA regulations.
- Supervise research staff and collaborate with multidisciplinary teams to ensure project milestones are met efficiently.
- Conduct quality assurance audits aligned with clinical trials management standards to uphold research integrity.
Skills
- Proven supervising experience in clinical or healthcare settings with strong leadership capabilities.
- Extensive knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques such as phlebotomy.
- Proficiency in data management software.
- Familiarity with FDA regulations, ICH GCP certification (or equivalent), and clinical research compliance requirements.
- Strong project management skills with experience overseeing multiple research projects simultaneously.
- Ability to review complex documentation accurately while ensuring adherence to clinical quality assurance standards.
- Excellent communication skills for effective collaboration within research teams and with external regulatory bodies.
Embark on a rewarding career that combines scientific rigor with compassionate patient care—where your expertise directly contributes to groundbreaking medical advancements!
Pay: $50,000.00 - $65,000.00 per year
Benefits:
- 401(k)
- Paid time off
Work Location: In person
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Where South Carolina roles are concentrated, by current openings.
Clinical Research Job Market in South Carolina
A snapshot from current South Carolina openings, updated as new roles post.
Who's Hiring
What South Carolina Employers Look For
The qualifications that appear most often in clinical research jobs across South Carolina.
- Relevant clinical research certification such as ACRP CCRC or SOCRA CCRP preferred or required
- Bachelor's degree in life sciences, nursing, pharmacy, or a related health discipline
- Minimum one to two years of direct clinical trial coordination or research experience
- Demonstrated knowledge of GCP guidelines, FDA regulations, and IRB submission processes
- Experience with electronic data capture systems such as Medidata Rave or REDCap
- Strong written communication skills for protocol documentation, adverse event reporting, and sponsor correspondence
Clinical Research Jobs in South Carolina: Frequently Asked Questions
How do you become a clinical research in South Carolina?
South Carolina does not require a state-issued license to work as a clinical research coordinator, so the path runs through education and nationally recognized certification. Most positions require at least a bachelor's degree in a life sciences or health-related field. From there, earning the ACRP Certified Clinical Research Coordinator credential or the SOCRA CCRP designation strengthens candidacy significantly. Many South Carolina academic medical centers, including MUSC Health and Prisma Health, post entry-level coordinator roles that serve as the standard starting point.
Which companies hire clinical researchs in South Carolina?
Employers hiring clinical researchs in South Carolina right now include Spartanburg Regional Healthcare System, Science 37, and Prisma Health, based on current listings on Migrate Mate as of August 2026. South Carolina's academic medical centers and contract research organizations tied to the state's pharmaceutical and biotech activity in the Charleston and Columbia corridors tend to post the most consistent volume.
Which South Carolina cities have the most clinical research jobs?
Greenville, Spartanburg, and Myrtle Beach have the most clinical research openings in South Carolina. Charleston leads because MUSC Health operates one of the Southeast's largest academic research programs, while Columbia's concentration of Prisma Health facilities and the University of South Carolina drives strong trial activity, and Greenville's growth as a regional medical hub has brought increasing research infrastructure to the Upstate.
Are there remote clinical research jobs in South Carolina?
Yes, but they're limited. About 33% of clinical research openings tied to South Carolina are remote or hybrid as of August 2026, reflecting the hands-on nature of most trial work. The roles most likely to offer remote or hybrid arrangements are regulatory affairs positions, data management roles, and sponsor-side monitoring jobs that do not require direct patient contact or on-site protocol execution.
How can I get hired as a clinical research in South Carolina with little or no experience?
The most realistic entry path is applying for a clinical research coordinator I or research assistant role at one of South Carolina's academic medical centers, which regularly hire candidates with a relevant bachelor's degree and no prior trial experience. MUSC Health and Prisma Health both run research departments that onboard new coordinators and provide GCP training internally. Candidates coming from adjacent roles such as medical assistant, phlebotomist, or clinical data specialist have a strong lateral case, and completing the ACRP Essentials certificate before applying gives an additional edge.
Where can I find and apply to clinical research jobs in South Carolina?
You can find and apply to clinical research jobs in South Carolina on Migrate Mate, which lists current openings from employers actively hiring in the state. Search the listings, identify the roles that match your experience and target area, and apply directly to the ones that fit.
See All 12 Clinical Research Jobs in South Carolina
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