Remote Part-Time Clinical Trial Coordinator (Medical Devices)

ACE Partners; United States; Hybrid; USD 34.000 - 55.000; Teilzeit

Zusammenfassung

ACE Partners partners with a medical device company to hire a Clinical Trial Coordinator (CTC) for the vascular space. This role supports day-to-day execution of clinical studies across sites, CROs, vendors and internal teams, with a focus on compliance and timely delivery.

The position is remote or hybrid and East Coast based, part-time up to 29 hours per week. You will help plan, start-up, maintain and close studies, manage TMF/eTMF, IRB submissions and site payments while ensuring GCP and FDA

Qualifikationen

• 2–5 years of clinical trial experience
• Medical device clinical trial experience preferred
• Working knowledge of GCP and FDA regulations
• Experience with EDC and TMF/eTMF systems preferred

Aufgaben

• Support study planning, coordination and tracking
• Coordinate with clinical sites, CROs, vendors and internal teams
• Support study start-up, maintenance and closeout activities
• Manage IRB/EC submissions and regulatory documentation
• Maintain TMF/eTMF and study documentation
• Track site payments, budgets, contracts and device inventory
• Assist investigator meetings, study training and committee logistics
• Data tracking, reconciliation and quality control
• Ensure activities comply with GCP, FDA regulations and internal procedures

Kenntnisse

Clinical trial coordination

GCP/FDA knowledge

Project coordination

Excellent attention to detail

Communication skills

Tools

EDC software

TMF/eTMF systems

Jobbeschreibung

ACE Partners partners with a medical device company to hire a Clinical Trial Coordinator (CTC) for the vascular space. This role supports day-to-day execution of clinical studies across sites, CROs, vendors and internal teams, with a focus on compliance and timely delivery.

The position is remote or hybrid and East Coast based, part-time up to 29 hours per week. You will help plan, start-up, maintain and close studies, manage TMF/eTMF, IRB submissions and site payments while ensuring GCP and FDA