Job Description
Join Mayo Clinic's world-renowned research team as a Clinical Research Coordinator. Shape the future of medicine by managing groundbreaking studies in our state-of-the-art facilities. We offer comprehensive benefits, professional development, and a collaborative environment where innovation thrives. Your work will directly impact patient care and medical breakthroughs.
Responsibilities
- Design and implement clinical trial protocols ensuring regulatory compliance and ethical standards
- Recruit, screen, and enroll participants while maintaining accurate documentation
- Monitor trial progress, collect data, and ensure protocol adherence
- Collaborate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Prepare regulatory submissions and maintain IRB compliance documentation
- Analyze and report trial outcomes with precision and attention to detail
- Train staff on research protocols and Good Clinical Practice (GCP) standards
Qualifications
- Bachelor's degree in life sciences, nursing, or related field (Master's preferred)
- 2+ years clinical research coordination experience in GCP environment
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in FDA regulations, ICH-GCP, and HIPAA compliance
- Advanced proficiency in electronic data capture systems (e.g., Medidata Rave)
- Exceptional organizational skills with ability to manage multiple protocols
- Strong written and verbal communication skills for stakeholder interactions