Senior Site Activation Specialist (Sponsor Dedicated)
Core
End-to-end site start-up activities for clinical trials, supporting site identification, feasibility, activation, and ongoing maintenance across multiple sponsors and therapeutic areas.
Role type
Senior Site Activation Specialist (Clinical Trials)
Builds
Clinical trial sites ready for patient enrollment
Domain
Life Sciences / Clinical Research
Required skills
Site feasibility and identification, Ethics submission management, Informed consent form (ICF) coordination, Site budget and contract negotiation, Project tracking and system maintenance, Risk and timeline communication
Preferred skills
Mentoring less experienced team members, Operating with high autonomy
Technologies
Internal project trackers, Ethics submission systems
Responsibilities
Support site feasibility, site identification, site start-up, and maintenance activities; Prepare, review, and track site start-up documentation; Act as key point of contact for investigative sites; Independently coordinate ethics and ICF submissions; Lead site budget and contract negotiations; Maintain accurate site and study information; Provide operational guidance and informal mentoring.
Seniority
Senior, hands-on IC
