On-Site Clinical Research Assistant — Daytona Beach

CVAUSA; Florida; On-site; USD 42,000 - 54,000; Full time

Job summary

CVAUSA seeks a Clinical Research Assistant to provide on-site support in Daytona Beach, FL. You will assist CRCs, investigators, and study teams with scheduling, specimen handling, and documentation to ensure smooth study conduct.

Responsibilities include coordinating visits, managing supplies, processing specimens, and maintaining logs and regulatory files, supporting protocol adherence and sponsor requirements.

Qualifications

• High school diploma required; health science degree preferred.
• Current or previous pharmacy technician experience required.
• Experience handling specimens or laboratory procedures preferred.
• Strong organizational and communication skills essential.

Responsibilities

• Coordinate participant appointments and study visits.
• Assist with visit preparation and participant flow.
• Maintain study calendars and visit schedules.
• Support participant retention activities.
• Maintain research supplies and track inventory.
• Process biological specimens according to protocol.
• Prepare and package specimens for shipment and recordkeeping.
• Maintain temperature logs and equipment monitoring records.
• Assist with document collection, filing, and regulatory binders.
• Escalate deviations and participate in quality improvement activities.

Skills

Strong organizational skills

Ability to manage multiple priorities

Attention to detail and accuracy

Strong communication and customer se r

Education

High school diploma required

Associate's or bachelor's degree preferred

Tools

Microsoft Office

CTMS

EDC

Sponsor systems

Job description

CVAUSA seeks a Clinical Research Assistant to provide on-site support in Daytona Beach, FL. You will assist CRCs, investigators, and study teams with scheduling, specimen handling, and documentation to ensure smooth study conduct.

Responsibilities include coordinating visits, managing supplies, processing specimens, and maintaining logs and regulatory files, supporting protocol adherence and sponsor requirements.