Job Description
Join Mayo Clinic's prestigious Department of Clinical Research and contribute to groundbreaking medical advancements. We seek a meticulous Senior Clinical Research Coordinator to oversee complex oncology trials, ensuring protocol compliance and data integrity. This role offers unparalleled opportunities to collaborate with world-renowned physicians and contribute to life-saving therapies in a state-of-the-art research environment.
Our ideal candidate thrives in dynamic, patient-focused settings and possesses exceptional organizational skills. Mayo Clinic provides comprehensive benefits, professional development opportunities, and a supportive culture dedicated to medical innovation.
Responsibilities
- Manage end-to-end clinical trial operations for Phase I-III oncology studies
- Ensure strict adherence to FDA regulations, GCP standards, and institutional protocols
- Recruit, screen, and enroll eligible participants with precision and compassion
- Maintain accurate electronic data capture systems and regulatory documentation
- Coordinate multidisciplinary teams including physicians, nurses, and biostatisticians
- Monitor adverse events and ensure timely reporting to IRB and sponsors
- Lead site initiation visits and routine audits for compliance verification
Qualifications
- Bachelor's degree in Nursing, Health Sciences, or related field (Master's preferred)
- 5+ years of clinical research coordination experience in oncology
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proven expertise with electronic data capture systems (e.g., Medidata Rave)
- Exceptional knowledge of FDA regulations and ICH-GCP guidelines
- Strong analytical skills with attention to detail in data management
- Excellent interpersonal abilities for patient communication and team collaboration
- Ability to manage multiple complex timelines simultaneously