Senior Clinical Research Coordinator - Cardiovascular
DM Clinical Research · Posted Nov 12, 2026
- Tomball, Texas, United States
- On-site
- Full-time · Senior
- 4–5 years
Coordinate cardiovascular clinical research studies at assigned investigative sites, ensuring compliance with protocols, regulations, and sponsor expectations.
Responsibilities
- Complete required training and certifications
- Conduct study subject visits and protocol-required procedures
- Document and enter data, resolve queries
- Maintain compliance with FDA regulations and ICH-GCP guidelines
- Liaise with laboratory, data, administrative staff, investigators, and CROs
Requirements
- High School Diploma or equivalent
- Bachelor's degree in a related health science discipline or Foreign Medical Graduate
- Nice to have: ACRP certification