Clinical Research Coordinator (Nurse Practitioner/ Physician Assistant)

Job Description

Job Description

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.