What are the responsibilities and job description for the Clinical Research Coordinator - 254662 position at Medix™?
Role: Clinical Research Coordinator - 6 month Contract assignment, 18 hours a week
Location: Onsite - Gulf Breeze, FL 32561
- Relocation candidates will NOT be considered for this position
Therapeutic Area: Dravet Syndrome (epilepsy / seizures)
Employment Type: Position is a contract, project based support role - current contract duration is estimated to be 6 months, possibility for extension depending on project needs
Schedule/ Shift:
- 18 hours a week (open to reviewing candidates' preferred work schedules)
- M-F during daytime business hours - NO evenings/weekends
Responsibilities/ Job Duties:
We are seeking a detail-oriented Clinical Research Coordinator (CRC) with a strong focus on prescreening and recruitment to support the successful execution of a Dravet Syndrome trial. This role will focus heavily on patient prescreening, recruitment, outreach and follow up activities, ensuring qualified participants are identified and engaged in accordance with study protocols.
The CRC will collaborate with investigators, healthcare providers, and study participants while maintaining accurate documentation, regulatory compliance, and high-quality clinical research standards. Strong communication, organizational skills, and experience in patient recruitment are essential for success in this role.