Job Description
Join our pioneering team at MediGen Health Solutions, where innovation meets compassionate care. We're seeking a dedicated Senior Clinical Research Coordinator to drive groundbreaking studies in oncology and immunotherapy. You'll collaborate with world-class physicians, manage complex protocols, and contribute to life-changing medical advancements. Enjoy comprehensive benefits, professional development opportunities, and a supportive environment that values your expertise.
Responsibilities
- Oversee clinical trial protocols from initiation to closure, ensuring FDA/GCP compliance
- Recruit and screen participants while maintaining ethical standards and informed consent processes
- Coordinate multidisciplinary teams including physicians, nurses, and data specialists
- Monitor patient safety, adverse events, and protocol deviations with meticulous documentation
- Analyze and interpret clinical data for regulatory submissions and publication
- Maintain IRB submissions and ensure continuous compliance with ethical guidelines
Qualifications
- Master's degree in Nursing, Public Health, or Clinical Research with 5+ years' experience
- Certified Clinical Research Professional (CCRP) or equivalent certification required
- Proven expertise in oncology clinical trials and oncology-specific protocols
- Advanced proficiency in EDC systems (e.g., Medidata Rave) and regulatory documentation
- Exceptional communication skills with ability to translate complex medical concepts
- Strong project management capabilities with demonstrated success in multi-center trials