Clinical Research Nurse Practitioner / Physician Assistant

Monroe+Biomedical+Research • North Charleston, SC

9d • Onsite

About The Position

Monroe Biomedical Research (MBR) is seeking an experienced, patient-focused Clinical Research Nurse Practitioner/Physician Assistant to join their Charleston team. This role combines advanced clinical practice with clinical research, involving participant screening, enrollment, study visits, clinical assessments, documentation, and follow-up. The position is ideal for an NP or PA who thrives in a fast-paced clinical environment, values compassionate, patient-centered care, and is passionate about advancing medicine through clinical research.

Requirements

• Current Nurse Practitioner (NP) or Physician Assistant (PA) licensure, with the ability to provide care to an adult patient population.
• Master’s degree in nursing, physician assistant studies, or a related advanced practice field from an accredited institution, as applicable to the role.
• Previous direct patient care experience required.
• Strong clinical judgment and demonstrated commitment to patient safety.
• Excellent organizational, documentation, and attention-to-detail skills.
• Ability to interpret and follow detailed clinical trial protocols and regulatory requirements.
• Ability to manage competing priorities and multiple studies in a fast-paced research environment.
• Strong communication and interpersonal skills with a compassionate, patient-centered approach.

Nice To Haves

• Clinical research experience is highly preferred.

Responsibilities

• Coordinate and manage clinical trial activities from participant screening through study completion.
• Review study protocols and ensure all required procedures, assessments, and visits are completed accurately and within established timelines.
• Develop and maintain complete, accurate source documentation in accordance with study protocols and regulatory requirements.
• Support participant recruitment, screening, enrollment, and ongoing study activities.
• Collaborate with investigators, sponsors, clinical research monitors, and internal team members to ensure efficient study execution.
• Ensure clinical trials are conducted in compliance with Good Clinical Practice (GCP), FDA regulations, sponsor requirements, and internal standard operating procedures.
• Provide clinical assessments and care to adult study participants within the scope of NP/PA practice and applicable study protocols.
• Perform and/or oversee study-related clinical procedures, including blood draws, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments.
• Review participants’ medical histories, medications, laboratory results, and other relevant clinical information.
• Educate participants on study requirements, procedures, medications, and follow-up expectations.
• Recognize and communicate changes in participant health, adverse events, and other clinically significant findings to the appropriate study team members.
• Deliver a professional, compassionate, and supportive experience throughout each participant’s clinical trial journey.
• Review and process medical records and clinical research documentation.
• Accurately document study visits, clinical assessments, and relevant findings.
• Enter and maintain study data in sponsor-provided and clinical research systems within required timelines.
• Prepare, process, and coordinate laboratory specimen shipments in accordance with protocol requirements.
• Respond to data queries and support the maintenance of complete, accurate, and inspection-ready study records.

Benefits

• 100% company-paid employee health, dental, and vision insurance.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level