Job Description
Join Mayo Clinic's prestigious Cardiology Research Division as a Senior Clinical Research Coordinator. Lead groundbreaking trials in cardiovascular therapeutics while collaborating with world-renowned physicians. We offer cutting-edge resources, comprehensive benefits, and opportunities for professional growth in a patient-centered environment.
Mayo Clinic is ranked #1 in cardiology by U.S. News & World Report. This role provides mentorship opportunities and competitive compensation including relocation assistance and continuing education stipends.
Responsibilities
- Design and implement complex clinical trial protocols for cardiovascular studies
- Monitor patient recruitment progress and ensure compliance with FDA/ICH-GCP standards
- Manage electronic data capture systems and maintain accurate regulatory documentation
- Coordinate cross-functional teams including physicians, biostatisticians, and regulatory affairs specialists
- Analyze adverse event reports and prepare safety submissions to IRB/ethics committees
- Present findings at national conferences and contribute to peer-reviewed publications
Qualifications
- Master's degree in Nursing, Public Health, or related clinical field (BSN with 5+ years experience considered)
- Certified Clinical Research Professional (CCRP) or ACRP-CP certification required
- Minimum 4 years coordinating multi-center clinical trials in cardiology or oncology
- Proficiency in clinical trial management systems (e.g., Medidata Rave, Veeva Vault)
- Strong knowledge of 21 CFR Parts 11, 312, and 812 regulations
- Experience managing budgets exceeding $500K in clinical research grants
- Excellent written communication skills for protocol development and regulatory submissions