Job Description
Join Mayo Clinic's prestigious research division as a Senior Clinical Research Coordinator. Lead groundbreaking clinical trials in cardiovascular medicine while mentoring junior staff and ensuring regulatory compliance. This role offers unparalleled opportunities to contribute to life-saving research initiatives in a state-of-the-art medical environment.
Responsibilities
- Design and oversee complex clinical trial protocols adhering to FDA and GCP standards
- Manage site initiation, patient recruitment, and data collection processes
- Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Prepare regulatory submissions and maintain audit-ready documentation
- Mentor junior coordinators and conduct protocol training sessions
- Analyze trial data and prepare comprehensive study reports for sponsors
- Implement risk-based monitoring strategies to ensure data integrity
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years of clinical research coordination experience in cardiology
- Certified Clinical Research Professional (CCRP) certification required
- Proven expertise in FDA regulations, ICH-GCP, and 21 CFR compliance
- Advanced proficiency in EDC systems (e.g., Medidata Rave) and statistical software
- Exceptional project management skills with ability to handle multiple trials
- Strong leadership experience in mentoring research teams
- Excellent written communication for regulatory document preparation