Job Description
Join our pioneering clinical research team at MediVance Research Institute, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to lead groundbreaking trials in oncology therapeutics. Enjoy competitive compensation, comprehensive benefits, and the opportunity to shape the future of medicine in our state-of-the-art facilities.
Responsibilities
- Design and implement complex clinical trial protocols in accordance with FDA and ICH-GCP standards
- Manage site operations including patient recruitment, data collection, and regulatory submissions
- Lead cross-functional teams of physicians, nurses, and data specialists
- Conduct site monitoring visits and ensure protocol compliance
- Analyze trial data and prepare comprehensive study reports for regulatory bodies
- Maintain electronic medical records and ensure data integrity
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years of clinical research coordination experience in oncology
- Certified Clinical Research Professional (CCRP) certification required
- Proven expertise in FDA 1572 and IND documentation
- Advanced proficiency in electronic data capture systems (e.g., Medidata Rave)
- Strong knowledge of HIPAA and GCP compliance
- Exceptional project management and leadership skills