Clinical Research Coordinator (Nurse Practitioner/ Physician Assistant)

Clinical Research Coordinator (Nurse Practitioner/ Physician Assistant)
Location: Charleston, SC (Onsite)
About Monroe Biomedical Research
Monroe Biomedical Research is one of the highest-performing clinical research centers in the country, conducting clinical trials to investigate treatments for asthma, COPD, heart failure, diabetes, and COVID-19.
With plans to expand operations over the next 6–12 months, we are seeking motivated Nurse Practitioners and Physician Assistants who are interested in contributing to cutting-edge clinical research and helping advance the development of next-generation therapies.
Position Overview
We are looking for a dedicated and hardworking Nurse Practitioner or Physician Assistant with experience performing infusions, physical examinations, and other study-related medical procedures. The ideal candidate will be comfortable working in a fast-paced clinical research environment and providing quality care to clinical trial participants.
Key Responsibilities
Perform clinical trial procedures and collect accurate patient data.
Administer injections, immunizations, infusions, and other medical procedures as required by study protocols.
Assess participant health through patient interviews, physical examinations, and electrocardiograms (ECGs).
Review, document, and process medical records.
Support clinical research protocols while maintaining patient safety and data accuracy.
Work collaboratively with research staff and clinical trial participants.
Qualifications and Requirements
Must have current South Carolina licensure as a Physician Assistant or Nurse Practitioner.
Current NCCPA certification for Physician Assistants or appropriate certification for Nurse Practitioners.
Previous clinical research experience is preferred; candidates with a strong interest in transitioning into clinical research are encouraged to apply.
Familiarity with medical instruments, equipment, and clinical procedures.
Ability to adapt to changing study demands and perform procedures on an as-needed basis.
Ability to work fully onsite in Charleston, SC,
Ideal Candidate
Excellent interpersonal and communication skills, with the ability to build rapport with clinical trial participants.
Friendly, outgoing, tactful, and professional demeanor.
Ability to work independently and collaboratively within a multidisciplinary team.
Strong attention to detail and commitment to patient safety.
Interest in long-term career growth within the clinical research industry.
Salary and Benefits
Competitive, negotiable salary based on experience.
Performance-based commission opportunities.
Company-matched 401(k) plan.
Medical, dental, and vision insurance, with premiums fully covered by the company.
Opportunities for career advancement and leadership development within the first 1–2 years.

Employment type
Full-Time

Work arrangement
No