Job Description
Join MedTech Innovations, a leader in pioneering medical research, as a Clinical Research Coordinator. You'll be instrumental in advancing breakthrough treatments while ensuring regulatory compliance and patient safety. Collaborate with multidisciplinary teams to drive innovation in life-changing therapies. We offer competitive benefits, professional development opportunities, and a dynamic work environment dedicated to improving global health outcomes.
Responsibilities
- Design and implement clinical trial protocols in compliance with FDA and GCP standards
- Recruit, screen, and enroll eligible study participants while maintaining ethical standards
- Manage trial data collection, verification, and reporting using electronic systems
- Coordinate investigator meetings, audits, and regulatory submissions
- Maintain accurate documentation including case report forms and regulatory binders
- Liaise with IRBs, sponsors, and study sites to ensure protocol adherence
- Monitor adverse events and ensure timely safety reporting
Qualifications
- Bachelor's degree in Nursing, Life Sciences, or related field (Master's preferred)
- 3+ years of clinical research coordination experience in therapeutic areas
- Certified Clinical Research Professional (CCRP) or equivalent certification
- Proficiency in EDC systems (e.g., Medidata Rave) and regulatory databases
- Strong knowledge of FDA regulations, ICH-GCP, and 21 CFR Part 11
- Exceptional organizational skills with attention to detail
- Excellent communication abilities for stakeholder interactions
- Ability to manage multiple concurrent trials in a fast-paced environment