Sr Site Activation Coordinator
Core
Perform site activation activities for investigative sites in assigned clinical studies, ensuring regulatory document completeness and accuracy.
Role type
Site Activation Coordinator
Builds
Regulatory and contractual documents for clinical trial sites
Domain
Clinical research / Life sciences
Required skills
Regulatory document preparation, SOP adherence, document review for accuracy, internal system/database maintenance, project tracking, multi-project management
Preferred skills
Life sciences degree, healthcare environment experience, MS Office proficiency
Responsibilities
Review regulatory documents for completeness and accuracy, distribute completed documents to sites and internal teams, track approval and execution of Investigator Packs and Informed Consent Forms, update internal project plans and timelines
Seniority
Entry-level, individual contributor
