Job Description
Join Boston Medical Center's prestigious Clinical Research Institute as a Clinical Research Coordinator and drive breakthroughs in patient care. We're seeking a meticulous professional to manage pivotal clinical trials while ensuring regulatory compliance and ethical integrity. This role offers unparalleled exposure to cutting-edge treatments in oncology, cardiology, and neurology within an NCI-designated comprehensive cancer center. Collaborate with world-class physicians, contribute to life-changing research, and advance your career in one of America's top healthcare systems.
Responsibilities
- Oversee all aspects of clinical trial protocols from initiation to closure, including patient recruitment, screening, and enrollment
- Maintain precise documentation of trial data in compliance with FDA, GCP, and institutional guidelines
- Coordinate with multidisciplinary teams including physicians, nurses, and biostatisticians
- Prepare and submit regulatory documents to IRB and sponsors with meticulous attention to detail
- Monitor adverse events and ensure timely safety reporting protocols
- Train site staff on trial procedures and regulatory requirements
- Analyze trial data and prepare comprehensive progress reports for stakeholders
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field required; Master's preferred
- Certified Clinical Research Professional (CCRP) or SOCRA certification required
- Minimum 3 years of clinical trial coordination experience in academic/hospital setting
- Proven expertise in oncology trial protocols highly desirable
- Advanced proficiency in electronic data capture systems (e.g., REDCap, Medidata Rave)
- Exceptional knowledge of ICH-GCP, FDA 21 CFR Part 812, and HIPAA regulations
- Strong analytical skills with experience in statistical data interpretation
- Excellent interpersonal skills for effective patient and stakeholder communication