Job Description
Join our pioneering team at MediVance Research Institute, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to drive groundbreaking studies in oncology therapeutics. Lead multi-center trials, collaborate with top-tier medical professionals, and contribute to life-changing breakthroughs. Enjoy competitive compensation, comprehensive benefits, and a dynamic work environment in Boston's premier healthcare corridor.
Responsibilities
- Oversee end-to-end clinical trial execution from protocol development to final reporting
- Manage site relationships, regulatory submissions, and FDA compliance
- Lead data collection, analysis, and quality assurance processes
- Mentor junior coordinators and train staff on SOPs and GCP standards
- Collaborate with biostatisticians on protocol design and statistical analysis plans
- Present trial outcomes to stakeholders and regulatory bodies
Qualifications
- Master's degree in Clinical Research, Nursing, or related field
- 5+ years coordinating oncology or pharmaceutical trials
- Certified Clinical Research Professional (CCRP) certification required
- Expertise in FDA regulations, ICH-GCP, and 21 CFR Part 820
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
- Strong project management with multi-center trial experience
- Exceptional communication and leadership skills