Peregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. This individual will play a critical role in ensuring studies are executed efficiently, ethically, and in compliance with regulatory standards.
Key Responsibilities
Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups
Maintain regulatory binders and ensure compliance with GCP and IRB requirements
Assist with study start-up, monitoring visits, and close-out activities
Collect and enter clinical data accurately into EDC systems
Serve as a liaison between investigators, sponsors, and patients
Qualifications
Bachelor’s degree in Life Sciences or related field
2–4+ years of clinical research experience
Strong knowledge of GCP and clinical trial processes