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Clinical Research Coordinator Associate
1 month ago
Job Summary
The Clinical Research Coordinator Associate will be responsible for managing and implementing multiple research protocols at Stanford Hospital and Clinics. This role will work closely with Principal Investigators and other team members to ensure the efficient and compliant execution of clinical trials.
Key Responsibilities
- Prepare and submit initial study documents to the Institutional Review Board (IRB) in compliance with local, state, and federal regulations.
- Recruit, screen, and enroll subjects in accordance with good clinical practice guidelines.
- Collect, record, and maintain complete data files using good clinical practice and HIPAA regulations.
- Participate in data retrieval, reporting, and preparation of files and Case Report Forms for various studies.
- Interact with subjects to schedule diagnostic and research evaluation visits, perform study-related assessments, and collect blood samples.
- Maintain drug accountability, study supplies, and equipment.
- Oversee subject compliance to the study protocol and report any changes in medications or adverse events to physicians.
- Report all serious adverse events promptly to investigators, sponsors, and the IRB.
Requirements
- Two-year college degree and two years of related work experience or a Bachelor's degree in a related field.
- Strong interpersonal skills and proficiency with Microsoft Office.
- Knowledge of medical terminology and certification from the Society of Clinical Research Associates or Association of Clinical Research Professionals is preferred.
Working Conditions
Occasional evening and weekend hours.
