GCO Associate I - Spain - FSP
Remote · Spain
Job Summary
GCO Associate I (iCRA) provides hands-on operational support for country and site clinical trial activities across start-up or conduct and close-out, maintaining trackers and timelines, following up on country/site deliverables, coordinating with local vendors/CROs, preparing and updating IRB/LEC submissions, and assisting with site contracting and essential document workflows. Works with local/regional clinical teams, Pfizer stakeholders, investigator sites, and external partners to ensure compliance with ICH/GCP and local regulatory requirements, while supporting study activation and ongoing study execution from a home-based office in Spain.
Required Qualifications
- BS/BA or bachelor’s degree in life sciences or a related discipline
- 2-5 years of relevant experience in clinical trial support, site activation, or clinical operations
- Exposure to country or site-level clinical trial operations and supporting documentation workflows
- Experience supporting contracting, regulatory, or vendor-related documentation processes is an advantage
- Fluent in English and local language (requirements apply by country); additional languages are an asset
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.