Clinical Research Coordinator II/III

Role: The Clinical Research Coordinator II/III manages and executes clinical research activities under the supervision of investigators, ensuring protocol compliance, data accuracy, and regulatory adherence. Responsibilities: Responsibilities include coordinating protocols, recruiting and screening participants, obtaining informed consent, collecting and recording data, performing patient assessments, managing study supplies, and overseeing adverse event reporting. The role involves data entry, maintaining study documentation, and supporting quality audits and inspections. Supervising support staff and training new team members are also key duties. Qualifications & Skills: Candidates should have at least 2 years of experience as a CRC in late-phase trials, with knowledge of GCP, FDA regulations, and biomedical research ethics. Strong interpersonal, communication, and organizational skills are essential. Proficiency in data management, regulatory compliance, and basic laboratory procedures is required. An associate or bachelor’s degree in healthcare or related fields, GCP certification, and experience with clinical trial software are mandatory. Additional Requirements: The role involves some travel, with shared company vehicles or reimbursement. Complementary benefits include health insurance, PTO, 401K, educational support, and more. The position emphasizes equal employment opportunity and adherence to legal and ethical standards.