Job Description
Join our pioneering team at Boston Medical Innovations, where cutting-edge research transforms patient care. We're seeking a meticulous Clinical Research Coordinator to drive our oncology clinical trials from protocol to publication. You'll collaborate with interdisciplinary teams to ensure regulatory compliance, patient safety, and data integrity while contributing to breakthrough therapies that save lives.
Our state-of-the-art facility in Boston's Medical District offers unparalleled resources for clinical research, including advanced molecular labs and a diverse patient population. This role provides mentorship from industry leaders and opportunities to present findings at international conferences.
Responsibilities
- Manage end-to-end clinical trial operations including protocol development, site initiation, and regulatory submissions
- Coordinate patient recruitment, enrollment, and retention strategies for oncology studies
- Maintain accurate electronic data capture systems and ensure GCP compliance
- Serve as primary liaison between investigators, sponsors, and IRB/ethics committees
- Analyze and report adverse events, protocol deviations, and study progress metrics
- Mentor junior staff and conduct investigator meetings for trial optimization
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in oncology trials
- Certified Clinical Research Professional (CCRP) or SOCRA certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
- Deep understanding of ICH-GCP, FDA regulations, and 21 CFR Part 11
- Exceptional attention to detail with demonstrated data management skills
- Strong written communication abilities for protocol development and reporting