Job Description
Join Mayo Clinic's prestigious Clinical Research Division as a Senior Clinical Research Coordinator. Lead groundbreaking studies in oncology, cardiovascular, or neurology research while ensuring protocol compliance and patient safety. Collaborate with multidisciplinary teams including physicians, biostatisticians, and regulatory experts. Enjoy comprehensive benefits, continuing education opportunities, and a culture of innovation.
Responsibilities
- Oversee complex clinical trials from initiation to closeout, maintaining ICH-GCP compliance
- Manage investigator sites, budgets, and regulatory documentation (FDA, IRB)
- Train and mentor junior coordinators on SOPs and trial protocols
- Analyze adverse events and ensure data integrity in electronic systems (e.g., Medidata Rave)
- Liaise with pharmaceutical sponsors to ensure protocol adherence and timely reporting
- Develop patient recruitment strategies and retention programs
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 5+ years clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Expertise in EDC systems and regulatory documentation management
- Strong knowledge of FDA 21 CFR Part 312 and ICH-GCP guidelines
- Exceptional communication skills for patient interactions and stakeholder management
- Experience with budget forecasting and financial tracking