Onsite Clinical Research Coordinator: Patient Care & Trials

Monroe Biomedical Research; Charleston (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

Monroe Biomedical Research in Charleston, SC seeks a patient-focused Clinical Research Coordinator onsite to oversee visits, screenings, and study procedures. This hands-on role blends direct patient care with trial coordination to advance medical research.

Experience in clinical research and nursing background is preferred; RN or NP licensure is required or preferred. You will work with investigators, sponsors, and staff, ensure protocol compliance, and maintain accurate documentation while

Qualifications

• Preferred current medical license or experienced in clinical research with the ability to practice with an adult patient population.
• Preferred Bachelor’s degree in nursing required; Master’s degree for NP candidates.
• Previous direct patient care experience required.
• Clinical research experience is highly preferred.
• Strong clinical judgment and commitment to patient safety.
• Excellent organization, documentation, and attention to detail.
• Ability to interpret and follow detailed clinical trial protocols.
• Ability to manage multiple priorities in a fast-paced environment.
• Strong communication and interpersonal skills.
• Professional, compassionate, and patient-focused approach.
• Must commute daily to Charleston, SC

Responsibilities

• Coordinate clinical trial visits from screening through completion.
• Review protocols and ensure study procedures are completed accurately and on schedule.
• Maintain complete and accurate source documentation.
• Support participant screening, enrollment, and ongoing study activities.
• Collaborate with investigators, sponsors, monitors, and research staff.
• Ensure compliance with GCP, FDA regulations, sponsor requirements, and internal procedures.
• Provide clinical assessment and care to adult study participants within your scope of practice and study requirements.
• Perform and/or oversee procedures including blood draws, ECGs, pulmonary function testing, vital signs, and other protocol-required assessments.
• Review medical history, medications, laboratory results, and other clinical information.
• Educate participants on study procedures, medications, and follow-up.
• Recognize and communicate adverse events or clinically significant findings.
• Deliver a professional, compassionate, and patient-centered experience.
• Document study visits, clinical findings, and patient information accurately.
• Enter and maintain study data within sponsor systems and required timelines.
• Process and coordinate laboratory specimens according to protocol.
• Respond to data queries and maintain accurate, inspection-ready records.

Skills

Direct patient care

Clinical research experience

Strong communication

Attention to detail

Education

Bachelor's degree in Nursing

Master's degree (NP)

Job description

Monroe Biomedical Research in Charleston, SC seeks a patient-focused Clinical Research Coordinator onsite to oversee visits, screenings, and study procedures. This hands-on role blends direct patient care with trial coordination to advance medical research.

Experience in clinical research and nursing background is preferred; RN or NP licensure is required or preferred. You will work with investigators, sponsors, and staff, ensure protocol compliance, and maintain accurate documentation while