Sr. Site Activation Specialist, IQVIA Biotech
Core
Execute country-level Site Activation activities for clinical research studies, managing feasibility, site identification, startup, and document execution to ensure sites are ready for trials.
Role type
Senior individual contributor clinical research specialist (Site Activation)
Builds
Activated clinical research sites ready for patient enrollment
Domain
Clinical research / Life sciences
Required skills
Clinical research operations, site feasibility assessment, regulatory compliance, document management, project timeline planning, quality control, stakeholder coordination
Preferred skills
Leadership experience, system/process improvement, local market expertise
Technologies
Internal clinical research databases, tracking tools, document management systems
Responsibilities
Serve as Single Point of Contact for investigative sites and project teams; Perform feasibility studies, site identification, and startup activities; Prepare and review site documents for completeness and accuracy; Track and follow up on regulatory and contractual document execution; Provide local expertise to Site Activation Managers and project teams; Conduct quality control of documents provided by sites.
Seniority
Senior, hands-on IC
