Job Description
Join Mayo Clinic's prestigious research division as a Clinical Research Coordinator, where innovation meets compassionate care. You'll play a pivotal role in advancing medical breakthroughs while ensuring protocol integrity and patient safety. This opportunity offers unparalleled mentorship in cutting-edge therapeutic areas including oncology and neurology.
Our state-of-the-art facilities and collaborative environment empower you to transform clinical trials into life-changing treatments. Mayo Clinic's commitment to excellence provides unmatched resources for professional growth and research impact.
Responsibilities
- Oversee complex clinical trial protocols from initiation to closeout
- Ensure strict compliance with FDA regulations and GCP standards
- Manage patient recruitment strategies and informed consent processes
- Coordinate multi-disciplinary research teams and vendor relationships
- Maintain accurate electronic data capture systems and regulatory documentation
- Analyze and interpret clinical data for study reports and publications
- Mentor junior research staff and implement process improvements
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years clinical research coordination experience in therapeutic area
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in FDA regulations, ICH-GCP, and clinical trial management
- Strong data management skills with EDC systems (e.g., Medidata Rave)
- Exceptional communication and stakeholder management abilities
- Proven track record in protocol development and site management