Job Description
Join Boston Medical Center's prestigious Research Institute as a Senior Clinical Research Coordinator and drive groundbreaking medical innovations. We seek a meticulous professional to manage complex oncology trials while ensuring regulatory compliance and patient safety. This role offers unparalleled opportunities to collaborate with world-renowned physicians and contribute to life-changing therapies.
Our dynamic team fosters continuous professional growth through industry-leading training programs and cutting-edge research facilities. Enjoy comprehensive benefits including malpractice coverage, generous PTO, and tuition reimbursement. Work in a mission-driven environment where your expertise directly impacts patient outcomes.
Responsibilities
- Oversee end-to-end execution of Phase II/III oncology clinical trials per FDA/ICH-GCP guidelines
- Manage electronic data capture systems and ensure protocol compliance through rigorous source document verification
- Lead site initiation visits, monitor study progress, and prepare regulatory submissions
- Coordinate multi-disciplinary teams including investigators, sponsors, and ethics committees
- Develop patient recruitment strategies and maintain comprehensive study documentation
- Analyze adverse events and ensure timely safety reporting to IRB and sponsors
- Mentor junior coordinators and optimize research workflows
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- 5+ years of oncology clinical trial coordination experience
- Expertise in electronic data capture systems (e.g., Medidata Rave, Oracle Inform)
- Proven track record in FDA audit readiness and regulatory compliance
- Strong data management and statistical analysis skills using SAS or R
- Excellent interpersonal skills with ability to navigate complex institutional hierarchies
- Current CPR/BLS certification