Job Description
Join our pioneering clinical research team at MediVance Innovations, where cutting-edge science meets compassionate patient care. We seek a meticulous Lead Clinical Research Coordinator to drive critical oncology trials at our Boston facility. This role offers the opportunity to shape the future of medicine while collaborating with world-class physicians, biostatisticians, and regulatory experts. Enjoy competitive compensation, comprehensive benefits, and a dynamic environment dedicated to medical breakthroughs.
Responsibilities
- Design and implement comprehensive clinical trial protocols for oncology studies
- Recruit, screen, and enroll qualified research participants with precision
- Manage all regulatory documentation ensuring FDA and GCP compliance
- Coordinate multi-disciplinary research teams across hospital departments
- Analyze and interpret complex clinical data using advanced statistical software
- Present findings at national conferences and peer-reviewed journals
- Mentor junior coordinators and maintain quality assurance systems
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- Certified Clinical Research Professional (CCRP) or equivalent certification
- 5+ years oncology trial coordination experience in academic/hospital setting
- Proven expertise in FDA 21 CFR Part 11 and ICH-GCP compliance
- Advanced proficiency in REDCap, Medidata Rave, and SAS
- Strong publication record in peer-reviewed medical journals
- Exceptional IRB interaction and audit management experience