Job Description
Join our prestigious medical research institute at the forefront of groundbreaking clinical trials. As a Clinical Research Coordinator, you'll drive innovation in patient care while working alongside world-class physicians and scientists. We offer a collaborative environment, cutting-edge resources, and opportunities for professional growth in one of America's most vibrant healthcare hubs.
Responsibilities
- Oversee all phases of clinical trials from protocol development to final report submission
- Ensure compliance with FDA regulations, GCP guidelines, and institutional protocols
- Manage patient recruitment, enrollment, and retention strategies
- Coordinate data collection, verification, and database management
- Liaise between investigators, sponsors, and regulatory bodies
- Monitor adverse events and maintain safety documentation
- Prepare regulatory submissions and maintain trial documentation
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- Minimum 3 years clinical research coordination experience
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in FDA regulations, ICH-GCP, and 21 CFR Part 820
- Strong proficiency in clinical trial management systems (e.g., Medidata Rave)
- Exceptional organizational and project management skills
- Excellent written and verbal communication abilities
- Experience with oncology trials highly desirable