Clinical Research Coordinator

Job overview

The Clinical Research Coordinator role is onsite in Lewisville, TX. Compensation is not specified. Prime Clinical Research is a clinical research site conducting trials intended to bring innovative treatments to patients. The role exists to coordinate day-to-day clinical trial operations while protecting participants and maintaining accurate, compliant study records. It contributes to high-quality trial conduct through participant coordination, regulatory documentation, sponsor and IRB communication, and protocol adherence.

What you'll do

• Coordinate clinical trial operations in compliance with FDA regulations and GCP guidelines
• screen, enroll, and monitor participants
• collect and maintain study data and source documentation
• serve as a contact for sponsors, IRBs, and participants
• prepare regulatory documents and protocol amendments
• conduct informed consent processes
• support audits and monitor visits
• ensure protocol adherence.

What we're looking for

Skills & competencies

clinical research coordinator

clinical trials

participant coordination

fda regulations

gcp

irb submissions

study documentation

lewisville tx

prime clinical research

edc systems

Work arrangement

• Weekend coverage required

Benefits & perks

• 401(k)
• employee discounts
• health insurance
• paid time off.

Why this role

Bachelor’s degree in a related field preferred; 1+ year of clinical research coordination or related clinical experience; ACRP or SOCRA certification is a plus.

About the employer

PRIME CLINICAL RESEARCH INC is hiring for this role. Industry: Offices of Physicians (except Mental Health Specialists). Sector: 62.