Daytona Beach On-Site Clinical Research Assistant

Cardiovascular Associates of America - CVAUSA; Daytona Beach (FL); Vor Ort; USD 42.000 - 56.000; Vollzeit

Zusammenfassung

Cardiovascular Associates of America - CVAUSA in Daytona Beach, FL, is seeking a Clinical Research Assistant to provide essential operational and participant support for clinical studies. This on-site role collaborates with CRCs, investigators, and study teams to manage scheduling, specimens, supplies, and documentation.

The position emphasizes accurate study documentation, regulatory compliance, and proactive coordination of visits, shipments, and logs to ensure efficient study conduct and

Qualifikationen

• High school diploma required.
• Associate's or bachelor's in health science preferred.
• Current or previous pharmacy technician experience is required.
• Experience handling specimens or laboratory procedures preferred.
• Strong organizational skills and attention to detail.

Aufgaben

• Coordinate participant appointments and study visits.
• Assist with visit preparation and participant flow.
• Maintain study calendars and visit schedules.
• Process and ship specimens, with accompanying documentation.
• Maintain temperature logs and equipment monitoring records.
• Assist with regulatory binders and study start-up/close-out activities.
• Support filing and organization of study records.

Kenntnisse

Organizational skills

Attention to detail

Communication

Multitasking

Teamwork

MS Office

CTMS familiarity

EDC familiarity

Ausbildung

High school diploma

Associate's or bachelor's in health sciences preferred

Tools

MS Office suite

CTMS

EDC

Sponsor systems

Jobbeschreibung

Cardiovascular Associates of America - CVAUSA in Daytona Beach, FL, is seeking a Clinical Research Assistant to provide essential operational and participant support for clinical studies. This on-site role collaborates with CRCs, investigators, and study teams to manage scheduling, specimens, supplies, and documentation.

The position emphasizes accurate study documentation, regulatory compliance, and proactive coordination of visits, shipments, and logs to ensure efficient study conduct and