About this role
Under general supervision the Clinical Research Coordinator (CRC) - Intermediate champions patient safety and protocol integrity while upholding the highest standards of patient care. The CRC communicates effectively to support the successful conduct of clinical trials and ensure quality outcomes. Responsibilities include screening and scheduling patients, coordinating all on-study activities, and maintaining compliance with study requirements. The CRC also participates in study teleconferences with sponsors and clinical research organizations to promote clear communication and continuity of information.
- Education: Bachelor's degree is required.
- Ability to communicate and liaise with research participants, research team members, and other relevant partner/key stakeholders.
- Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
- Demonstrated ability to monitor important and complex projects concurrently.
- Some knowledge of Federal regulations and ethical standards governing human subjects research (e.g., FDA, HIPAA, IRB processes).
- Basic understanding of Clinical trial design, methodology, and protocol requirements.
- Knowledgeable in Medical terminology, anatomy, and disease processes relevant to assigned studies.
- Proficient knowledge of adverse event reporting procedures and documentation standards.
- Adept understanding of the principles of informed consent and patient rights.
- Ability to use Electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to adhere to Institutional policies and standard operating procedures (SOPs).
- Skilled in patient screening, recruitment, and informed consent processes.
- Ability to conduct and document study visits according to protocol.
- Problem-solving and critical thinking for protocol deviations or logistical challenges.
- Collaboration and teamwork in multidisciplinary clinical and research environments.