Job Description
Join our dynamic team at MediTech Solutions as a Clinical Research Coordinator and drive groundbreaking medical innovations. We're seeking a meticulous professional to manage clinical trials, ensuring compliance with FDA protocols and ethical standards. This role offers the opportunity to work alongside leading physicians and researchers in a cutting-edge healthcare environment, directly impacting patient outcomes through rigorous scientific investigation.
Responsibilities
- Oversee all phases of clinical trials from protocol development to final report submission
- Recruit, screen, and maintain detailed patient records while ensuring HIPAA compliance
- Coordinate with investigative sites, sponsors, and regulatory bodies
- Monitor adverse events and ensure data integrity across study databases
- Prepare regulatory documents and maintain IRB submissions
- Analyze and interpret clinical data using statistical software
- Mentor junior staff and train new personnel on SOPs
Qualifications
- Bachelor's degree in Nursing, Biology, or related healthcare field (Master's preferred)
- 3+ years of clinical research coordination experience
- Certified Clinical Research Professional (CCRP) certification
- Proficiency with EDC systems (e.g., Medidata Rave, Oracle Inform)
- Strong understanding of ICH-GCP and FDA regulations
- Exceptional organizational and multitasking abilities
- Excellent written and verbal communication skills
- Ability to work flexible hours including occasional weekends