Job Description
Join a cutting-edge healthcare pioneer revolutionizing patient outcomes through innovative clinical trials. We're seeking a passionate Clinical Research Coordinator to drive critical medical research initiatives that shape the future of healthcare. Our state-of-the-art facility in Boston offers collaborative environments where your expertise directly impacts life-changing treatments.
Responsibilities
- Design, implement, and monitor clinical trial protocols ensuring FDA/GCP compliance
- Coordinate multi-disciplinary research teams across oncology, cardiology, and neurology divisions
- Manage patient recruitment, informed consent processes, and retention strategies
- Analyze complex medical data using REDCap and SAS for regulatory submissions
- Spearhold site audits and ensure flawless documentation for IRB approvals
- Mentor junior staff and optimize research workflows for 95% protocol adherence
Qualifications
- Master's degree in Clinical Research, Nursing, or related healthcare field
- 3+ years of clinical trial coordination experience in hospital settings
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in oncology and cardiology trial methodologies
- Advanced proficiency in electronic data capture systems and regulatory databases
- Exceptional problem-solving skills for protocol deviation resolution
- Strong background in HIPAA compliance and patient privacy protocols