Clinical Research Nurse Coordinator (RN)

Job Description

Job Description

Clinical Research Nurse Coordinator (RN)

Entry to Associate Level

Schedule: Full-Time | Monday–Friday
Reports To: Director of Research

About the Role

We are seeking a Registered Nurse who is interested in growing their career in clinical research . This role is ideal for an RN with some experience in clinical trials or research activities who is eager to deepen their research skill set in a supportive, team-based environment.

You will work closely with experienced research professionals and the Principal Investigator to support multiple clinical studies, including both FDA-approved and investigational therapies . While prior research experience is helpful, we are open to candidates who are earlier in their research career and motivated to learn.

Typical workload includes 3–5 active studies at a time, with structured support and onboarding provided.

What You’ll Do

• Support clinical research studies in compliance with FDA regulations, GCP, and sponsor protocols
• Serve as a key clinical resource for study participants, ensuring patient safety and ethical conduct
• Assist with study start-up, including protocol review, site readiness, and documentation
• Screen, educate, and enroll eligible participants per study criteria
• Coordinate and conduct study visits, including clinical assessments and procedures
• Lead the informed consent process under the guidance of the Principal Investigator
• Perform nursing procedures such as:
• • Vital signs
  • EKGs
  • Lab draws
  • IV placement and infusions
• Accurately document study activities in source records, regulatory binders, and study logs
• Enter and maintain study data in electronic or paper CRFs
• Identify and report adverse events, protocol deviations, and safety issues per guidelines
• Collaborate with internal teams, sponsors, and monitors as needed

What We’re Looking For

• Active RN license (required)
• Bachelor’s degree in Nursing or related field
• Some clinical research experience preferred (can include:
• • CRC exposure
  • Research assistant work
  • Industry-sponsored trials
  • Academic or hospital-based research)
• Strong clinical judgment and attention to detail
• Comfortable working independently while collaborating closely with a research team
• Interest in building a long-term career in clinical research

Preferred Experience (Not Required)

• 1–3 years of clinical research or research-adjacent experience
• Experience with infusion-based or interventional studies
• Familiarity with GCP and human subject protection
• Experience working in outpatient or specialty clinic settings

Certifications

• RN & CPR (required)
• GCP certification (preferred; can be obtained if not current)
• IATA or other research-related certifications a plus
• CCRC welcome but not required

Avery Partners collaborates with businesses all over the US to help streamline their hiring processes.

Company Description

Avery Partners collaborates with businesses all over the US to help streamline their hiring processes.