Job Description
Join Boston Medical Center's prestigious clinical research team and contribute to groundbreaking medical advancements. We seek a passionate Clinical Research Coordinator to oversee complex clinical trials, ensuring compliance with FDA regulations and ethical standards. This role offers the opportunity to work alongside world-renowned physicians and researchers in a dynamic, patient-centered environment.
Our state-of-the-art facilities and collaborative culture provide an ideal setting for professional growth. We offer competitive benefits, continuing education support, and opportunities to lead innovative studies that directly impact patient care. If you're driven by scientific curiosity and committed to improving health outcomes, we invite you to apply.
Responsibilities
- Design and implement comprehensive clinical trial protocols aligned with FDA and ICH-GCP guidelines
- Recruit, screen, and enroll participants while maintaining strict ethical standards
- Manage electronic data capture systems and ensure data integrity throughout study phases
- Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Prepare regulatory submissions and maintain meticulous study documentation
- Monitor adverse events and ensure timely reporting to IRB and sponsors
- Analyze trial data and prepare comprehensive progress reports for stakeholders
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- Minimum 3 years clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in electronic data capture systems (e.g., Medidata Rave)
- Demonstrated knowledge of FDA regulations, ICH-GCP, and HIPAA compliance
- Exceptional organizational skills with attention to detail in documentation
- Strong interpersonal skills for patient communication and team collaboration
- Experience managing complex budgets and vendor relationships