Job Description
Join Boston Medical Center's prestigious research division as a Clinical Research Coordinator and drive groundbreaking medical innovations. We seek a meticulous professional to oversee complex clinical trials, ensuring compliance with FDA regulations and ethical standards. This pivotal role bridges scientific discovery with patient care, offering unparalleled growth in one of America's top healthcare ecosystems.
Enjoy comprehensive benefits including tuition reimbursement, flexible scheduling, and access to cutting-edge research facilities. Our collaborative environment fosters professional development through mentorship programs and industry conferences.
Responsibilities
- Manage and coordinate multi-phase clinical trials from protocol development to final report submission
- Ensure strict adherence to GCP guidelines, FDA regulations, and institutional IRB protocols
- Recruit, screen, and enroll participants while maintaining comprehensive study documentation
- Monitor adverse events and implement corrective actions per SOP requirements
- Collaborate with biostatisticians for data analysis and report preparation
- Train clinical staff on study protocols and regulatory compliance procedures
- Prepare regulatory submissions and maintain audit-ready documentation systems
Qualifications
- Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)
- Minimum 3 years clinical research coordination experience in FDA-regulated trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency with electronic data capture systems (e.g., Medidata Rave, REDCap)
- Demonstrated knowledge of ICH-GCP and 21 CFR regulations
- Exceptional organizational skills with attention to detail in documentation
- Strong interpersonal abilities for patient communication and team collaboration
- Experience with oncology or cardiovascular trials highly desirable