Job Description
Join our pioneering team at MediVita Health Systems, where innovation meets compassionate care. We're seeking a Clinical Research Coordinator to drive transformative studies that shape the future of medicine. In this pivotal role, you'll manage clinical trials from protocol to publication, ensuring regulatory compliance and data integrity while collaborating with multidisciplinary teams. Our state-of-the-art research facility offers cutting-edge resources and a culture that values professional growth and patient-centered impact.
Responsibilities
- Design and execute clinical trial protocols adhering to FDA/ICH-GCP standards
- Recruit, screen, and enroll participants with diverse medical backgrounds
- Monitor data collection integrity and maintain comprehensive trial documentation
- Liaise between investigators, sponsors, and regulatory bodies for seamless trial operations
- Analyze statistical data and prepare regulatory submissions and publications
- Mentor junior research staff and implement process improvement initiatives
Qualifications
- Master's degree in Clinical Research, Nursing, or Life Sciences
- 3+ years coordinating clinical trials with therapeutic area expertise
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in EDC systems (e.g., Medidata Rave, Oracle Inform)
- Demonstrated success in FDA/EMA regulatory compliance
- Exceptional interpersonal skills for stakeholder collaboration
- Strong statistical analysis experience with SAS or R