Site Activation Specialist
Core
Serve as a Single Point of Contact to perform feasibility, site activation, and maintenance activities for investigative sites in clinical trials, ensuring patients have access to safe and effective medication.
Role type
Site Activation Specialist
Builds
Clinical trial site networks and activation workflows
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Feasibility assessment, site activation, document review for completeness and accuracy, regulatory compliance (ICH/GCP), database and tracking tool management, project plan updates
Preferred skills
Knowledge of local regulations and SOPs, experience with clinical trial documents (CDAs, Informed Consent Forms, Investigator Packs)
Responsibilities
Review and distribute regulatory and contractual documents to sites, track approval and execution of study documents, update internal systems and project plans, follow up on site progress
Seniority
Junior to Mid-level, hands-on IC
