Sr Site Activation Specialist
IQVIA · Madrid, Spain
Clinical OperationsFull-timeCompany career page
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Role summary
Senior Site Activation Specialist role leading complex clinical trial projects across IQVIA's global network. The position involves site identification, feasibility assessment, regulatory submissions, and ensuring quality adherence to timelines and standard procedures in Spain.
What they're looking for
- Bachelor's degree in Life Sciences or related field
- Minimum 3-4 years clinical research experience with 1 year in leadership role
- Experience with ethics committee submissions, regulatory authority interactions, and site activation
- Knowledge of ICH/GCP guidelines, local regulations, and SOPs
- Strong problem-solving, negotiation, and communication abilities
- Capacity to manage multiple concurrent projects
What you'll be doing
- Lead complex site activation projects with oversight of feasibility, site identification, and study start-up activities
- Serve as single point of contact between investigative sites, project managers, and internal departments
- Prepare, review, and track regulatory and contractual documents including ethics submissions and informed consent forms
- Perform quality control on site-provided documents and monitor progress against project timelines
- Mentor junior staff and provide subject matter expertise and local guidance to regional and project teams
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.