Clinical Research Coordinator II, RN
Core
Conducts delegated clinical tasks and monitoring of research participants in accordance with Good Clinical Practices (GCP), ensuring protocol and regulatory compliance.
Role type
Senior IC Clinical Research Coordinator (RN)
Builds
Clinical trials and research studies
Domain
Healthcare + Clinical Research
Required skills
RN license, phlebotomy, IV insertion, adverse event identification, protocol compliance, data documentation, patient recruitment, regulatory knowledge (FDA/ICH), site monitoring coordination
Preferred skills
1 year prior Care Access experience, recent phlebotomy experience, ability to work independently, critical thinking, stakeholder communication
Technologies
EDC systems, IVRS, paper/e-source documents
Responsibilities
Prescreen study candidates and obtain informed consent; Perform phlebotomy, vital signs, ECGs, and administer investigational products; Monitor participants for adverse reactions and identify/report AEs/SAEs; Coordinate site visits and monitor visits with Sponsor/CRO; Maintain Investigational Product records and blinding; Recruit subjects and manage recruitment plans; Document data in real-time and resolve queries; Mentor CRC I peers.
Seniority
Senior, hands-on IC