Job Description
Join our pioneering team at Boston Medical Research Institute and lead transformative clinical trials that shape the future of medicine. We're seeking a Senior Clinical Research Coordinator to manage complex oncology studies, ensuring compliance with FDA regulations and ethical standards. You'll collaborate with multidisciplinary teams to advance life-saving treatments while mentoring junior staff.
Our institute combines cutting-edge technology with compassionate patient care in state-of-the-art facilities. Enjoy comprehensive benefits, professional development opportunities, and the chance to contribute to breakthrough therapies.
Responsibilities
- Design and execute oncology clinical trials protocol adherence
- Recruit and retain diverse patient cohorts for multi-center studies
- Monitor adverse events and ensure regulatory compliance (FDA, GCP)
- Lead IRB submissions and maintain study documentation
- Analyze clinical data and prepare regulatory submissions
- Mentor junior research staff and train new coordinators
- Collaborate with pharmaceutical partners on trial optimization
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years coordinating oncology clinical trials
- Certified Clinical Research Professional (CCRP) required
- Experience with electronic data capture systems (EDC)
- Proven track record in FDA regulatory compliance
- Exceptional attention to detail and documentation skills
- Strong leadership abilities in cross-functional teams
- Knowledge of biostatistics and clinical trial methodologies