Job Description
Join our pioneering team at NovoMed Research Institute, where innovation meets compassionate care. We're seeking a Senior Clinical Research Coordinator to drive breakthroughs in oncology therapeutics. This role offers unparalleled opportunities to shape the future of patient care while working alongside world-renowned physicians in state-of-the-art facilities.
Enjoy comprehensive benefits including premium health insurance, 401(k) matching, and continuing education stipends. Our culture emphasizes work-life balance with hybrid scheduling options.
Responsibilities
- Oversee multi-phase clinical trials ensuring protocol adherence and regulatory compliance
- Coordinate patient recruitment, screening, and informed consent processes
- Manage electronic data capture systems and maintain accurate trial documentation
- Lead cross-functional teams including physicians, nurses, and biostatisticians
- Analyze trial data and prepare comprehensive regulatory submissions
- Implement quality assurance measures and audit preparation
- Mentor junior research staff and conduct protocol training sessions
Qualifications
- Master's degree in Clinical Research, Nursing, or related health field
- 5+ years of clinical trial coordination experience in oncology
- ACRP or SOCRA certification required
- Proficiency in Medidata Rave and REDCap systems
- Demonstrated knowledge of FDA 21 CFR Part 312 guidelines
- Exceptional communication skills for stakeholder engagement
- Certified Clinical Research Professional (CCRP) preferred
- Experience with phase II/III oncology trials mandatory