Job Description
Join MedTech Innovations, a leader in cutting-edge medical research, as a Clinical Research Coordinator. We're revolutionizing patient care through groundbreaking clinical trials, and we need your expertise to ensure seamless execution. This role offers the opportunity to work with world-class researchers, state-of-the-art facilities, and directly impact healthcare innovation. Enjoy competitive benefits, professional development opportunities, and a collaborative environment where your skills make a tangible difference.
Responsibilities
- Oversee clinical trial protocols, ensuring FDA compliance and regulatory adherence
- Manage participant recruitment, screening, and informed consent processes
- Coordinate data collection, monitoring, and quality assurance procedures
- Liaise with investigators, sponsors, and ethics committees for protocol approvals
- Maintain accurate electronic and paper trial documentation systems
- Analyze interim data and prepare regulatory submissions
- Train staff on clinical trial procedures and safety protocols
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- Certified Clinical Research Professional (CCRP) or equivalent certification
- 3+ years' experience in clinical trial coordination or research
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Clinical)
- Demonstrated knowledge of ICH-GCP and FDA regulations
- Strong organizational and multitasking abilities in fast-paced environments
- Exceptional communication skills with diverse stakeholders