Study Coordinator - Winter Park, FLA
ProPharma Group · US
Clinical OperationsPart-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ProPharma Group seeks a Study Coordinator based in Winter Park, Florida to manage remote clinical trial site activities, including subject coordination, data management, and regulatory compliance. The role supports the full lifecycle of drug and device development programs.
What they're looking for
- Bachelor's degree or 2+ years of related clinical research experience
- Proficiency with Microsoft Office and web-based research platforms on PC
- Knowledge of ICH/GCP guidelines and FDA/IRB regulatory requirements
- Strong verbal and written communication skills
- Ability to work independently and collaboratively in a remote setting
- Critical thinking and strong organizational skills with multitasking capability
What you'll be doing
- Serve as primary contact for site communications, document submissions, and activity coordination
- Support subject recruitment, screening, and re-consenting activities
- Conduct protocol activities as directed by the Principal Investigator
- Perform data entry, monitor clinical databases, and respond to system queries
- Maintain documentation compliant with IRB and FDA policies
Privacy & handoff
This role links to ProPharma Group's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.