Site Coordinator
Core
Supports clinical study sites in trial activities including monitoring visits, patient enrollment, data entry, and regulatory document management.
Role type
Site Coordinator
Builds
Clinical trial operations for medical institutions/research centers
Domain
Clinical research / Life Sciences
Deliverable
client delivery
Required skills
ICH-GCP compliance, patient enrollment tracking, EDC data entry, adverse event reporting, investigational product handling, regulatory document management, contract negotiation support, audit preparation
Preferred skills
Degree in Life Science (Pharmacy, Nursing, Lab Analytics), 2+ years experience, fast-paced environment adaptability, problem-solving
Technologies
EDC systems
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