Job Description
Join Mayo Clinic's prestigious research division where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive transformative clinical trials that shape the future of medicine. In this pivotal role, you'll manage complex study protocols, ensure regulatory compliance, and collaborate with multidisciplinary teams to accelerate therapeutic breakthroughs. Mayo offers unparalleled resources, cutting-edge facilities, and a culture where your expertise directly impacts patient outcomes.
Responsibilities
- Design and execute clinical trial protocols ensuring FDA/ICH/GCP compliance
- Recruit, screen, and enroll study participants while maintaining ethical standards
- Manage electronic data capture systems and ensure data integrity
- Coordinate with IRB and regulatory bodies for protocol amendments and submissions
- Train clinical staff on study procedures and safety protocols
- Prepare comprehensive regulatory documentation and study reports
- Monitor adverse events and ensure timely safety reporting
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 3+ years clinical research coordination experience with therapeutic trials
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Expertise in FDA regulations, ICH-GCP, and 21 CFR compliance
- Proficiency in electronic data capture systems (e.g., Medidata Rave, REDCap)
- Strong project management skills with attention to detail
- Exceptional communication and stakeholder management abilities