Job Description
Join our pioneering team at Boston Medical Research Institute, where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive impactful studies in oncology and immunotherapy. As a key member of our translational research division, you'll contribute to breakthroughs that transform patient outcomes while working in state-of-the-art facilities alongside world-renowned physicians.
Our collaborative environment offers competitive benefits, professional development grants, and the opportunity to shape the future of precision medicine. If you're passionate about accelerating medical discoveries while maintaining the highest ethical standards, we encourage you to apply.
Responsibilities
- Oversee end-to-end clinical trial management including protocol development, site initiation, and regulatory compliance
- Coordinate patient recruitment, screening, and informed consent processes while maintaining HIPAA compliance
- Manage electronic data capture systems and ensure accurate documentation per FDA/ICH-GCP guidelines
- Serve as primary liaison between investigators, sponsors, and IRB committees
- Monitor adverse events and ensure timely safety reporting to regulatory authorities
- Mentor junior staff and conduct investigator meetings to ensure protocol adherence
- Analyze trial data and prepare comprehensive reports for FDA submissions and publications
Qualifications
- Master's degree in life sciences, nursing, or related field (Bachelor's with 5+ years experience considered)
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Minimum 3 years coordinating Phase I-III oncology trials in academic or hospital setting
- Expertise in FDA regulations, ICH-GCP, and 21 CFR compliance
- Proficiency in electronic data capture systems (e.g., Medidata Rave, Veeva Vault)
- Strong statistical literacy and experience with SAS or R for data analysis
- Demonstrated ability to manage complex multi-center trials with diverse stakeholder groups