Clinical Research Nurse Practitioner​/Physician Assistant

M  – Charleston, SC | Onsite

Monroe Biomedical Research (M ) is growing, and we are seeking an experienced, patient-focused Clinical Research Nurse Practitioner/Physician Assistant to join our Charleston team.

This unique opportunity combines advanced clinical practice with hands-on clinical research, allowing you to deliver direct patient care while contributing to the successful execution of clinical trials.

From participant screening and enrollment to study visits, clinical assessments, documentation, and follow-up, you will play an integral role in ensuring high-quality research and positive participant experience.

This 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.

• 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.

• 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.
• Clinical research experience is highly preferred.
• 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…