Job Description
Join Boston Medical Innovations as a Senior Clinical Research Coordinator and lead groundbreaking studies that transform patient care in oncology. Our dynamic team at the forefront of medical innovation seeks a passionate professional to oversee complex clinical trials from protocol design to final submission. Enjoy competitive benefits, cutting-edge resources, and a culture that prioritizes professional growth and work-life balance. Make a tangible impact on healthcare while advancing your career in one of America's premier medical hubs.
Responsibilities
- Design, implement, and monitor multi-site clinical trials ensuring compliance with FDA regulations and ICH-GCP standards
- Coordinate interdisciplinary teams including investigators, statisticians, and regulatory affairs specialists
- Manage complex data collection, analysis, and reporting using electronic data capture systems
- Serve as primary liaison between sponsors, research sites, and IRB/EC committees
- Develop and maintain comprehensive trial documentation including protocols, informed consent forms, and study reports
- Mentor junior coordinators and optimize research workflows through continuous process improvement
Qualifications
- Master's degree in Clinical Research, Nursing, Life Sciences, or related field (B.S. with 5+ years experience considered)
- 3+ years coordinating Phase II-III clinical trials in oncology or therapeutic area
- Certified Clinical Research Professional (CCRP) or ACRP certification required
- Expertise in electronic data capture systems (Medidata Rave, Oracle Inform) and regulatory documentation
- Proven success in managing multi-site trials with complex protocol requirements
- Exceptional organizational skills with ability to prioritize competing deadlines
- Strong written communication for preparing regulatory submissions and study reports