Job Description
Join our pioneering team at MediTech Innovations where we're revolutionizing patient care through cutting-edge clinical research. As a Clinical Research Coordinator, you'll play a pivotal role in advancing medical breakthroughs while ensuring regulatory compliance and patient safety. We offer a collaborative environment with state-of-the-art facilities and opportunities for professional growth.
Responsibilities
- Oversee all phases of clinical trials from protocol development to final reporting
- Recruit, screen, and enroll eligible study participants with precision
- Manage regulatory documentation and ensure FDA/GCP compliance
- Coordinate with multidisciplinary teams including physicians, nurses, and data specialists
- Monitor adverse events and maintain accurate patient records
- Analyze trial data and prepare comprehensive study reports
- Maintain IRB approvals and ethical research standards
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Expertise in FDA regulations, ICH-GCP, and HIPAA compliance
- Exceptional organizational skills with attention to detail
- Strong proficiency in EDC systems (e.g., Medidata Rave)
- Excellent communication and stakeholder management abilities