Job Description
Join Mayo Clinic's prestigious research division and lead groundbreaking clinical trials that transform patient care. As a Senior Clinical Research Coordinator, you'll manage complex oncology studies from protocol development to FDA submission, ensuring GCP compliance and data integrity. Collaborate with multidisciplinary teams including physicians, biostatisticians, and regulatory experts to accelerate therapeutic innovations. Mayo Clinic offers unparalleled resources, cutting-edge facilities, and a culture where your expertise directly impacts global healthcare outcomes.
Responsibilities
- Design and implement clinical trial protocols for oncology studies
- Oversee site operations, including IRB submissions, informed consent, and budget management
- Train and mentor junior staff on regulatory compliance (FDA, ICH-GCP)
- Analyze complex datasets and prepare regulatory submissions
- Liaise with pharmaceutical sponsors and CROs on trial progress
- Present findings at scientific conferences and peer-reviewed journals
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years of clinical trial coordination experience in oncology
- Certified Clinical Research Professional (CCRP) certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Experience managing FDA audits and regulatory inspections
- Strong statistical knowledge and SAS programming skills
- Exceptional project management and stakeholder communication abilities