Job Description
Join our pioneering team at MediTech Innovations, where cutting-edge medical research meets compassionate patient care. We're seeking a Clinical Research Coordinator to drive impactful studies in oncology and rare diseases. Enjoy a collaborative environment with state-of-the-art facilities, competitive benefits, and opportunities to shape the future of medicine.
Responsibilities
- Manage clinical trials from protocol development to close-out, ensuring FDA/GCP compliance
- Recruit, screen, and enroll study participants while maintaining ethical standards
- Coordinate multidisciplinary teams including physicians, nurses, and regulatory specialists
- Maintain accurate electronic medical records and regulatory documentation
- Analyze trial data and prepare reports for IRB submissions and sponsor reviews
- Monitor patient safety protocols and adverse event reporting procedures
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years clinical research coordination experience with oncology trials
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in EDC systems (e.g., Medidata Rave) and regulatory databases
- Demonstrated knowledge of ICH-GCP, FDA regulations, and HIPAA compliance
- Exceptional organizational skills with attention to detail and documentation
- Strong written/verbal communication abilities for cross-functional collaboration