Coordinate clinical trial activities, ensure compliance with regulations, maintain regulatory binders, collect and enter data, and liaise between stakeholders.
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
- Excellent organizational and interpersonal skills
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