Job Description
Join Mayo Clinic's prestigious clinical research division as a Senior Clinical Research Coordinator. You'll lead pivotal trials in oncology, drive protocol development, and ensure regulatory compliance while mentoring junior staff. Collaborate with world-class physicians and contribute to groundbreaking medical innovations.
Responsibilities
- Design and oversee complex clinical trial protocols in oncology research
- Manage regulatory submissions and ensure FDA/ICH-GCP compliance
- Train and supervise 3+ junior research coordinators
- Collaborate with biostatisticians on data analysis and reporting
- Develop informed consent documents and patient education materials
- Monitor adverse events and maintain accurate trial documentation
Qualifications
- Master's degree in Life Sciences, Nursing, or related field
- 5+ years clinical research coordination experience in oncology
- ACRP or SOCRA certification required
- Expertise in electronic data capture systems (e.g., Medidata Rave)
- Strong knowledge of FDA 21 CFR Part 11 and ICH-GCP guidelines
- Experience managing multi-center trials with $500k+ budgets