Site Activation Specialist
Core
Support the start-up and activation of clinical trial sites, ensuring efficient and compliant study launches.
Role type
Site Activation Specialist
Builds
Clinical trial studies for life sciences sponsors
Domain
Clinical research / Life sciences
Required skills
Feasibility assessment, regulatory documentation management, contract management, stakeholder coordination, internal system maintenance, compliance monitoring
Preferred skills
Experience in Pharmacovigilance (SAE reporting, Security Reports, CIOMs, Safety Reporting Packages)
Technologies
Internal study databases, tracking tools, study plans
Responsibilities
Support feasibility assessments and site activation activities; Serve as primary contact for investigative sites; Prepare and manage study documentation (CDAs, ICFs, Investigator Packs); Coordinate regulatory and ethics documentation; Monitor document review and approval status; Maintain project information in internal systems; Communicate site progress to stakeholders.
