When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
If you want to be part of a leading CRO and transform scientific discoveries into new treatments, then Parexel FSP challenges you to live up to your potential by joining us at GCO Associate I (iCRA) , home-based and sponsor dedicated, in Spain, Israel and Poland.
GCO Associate provides hands-on operational support for country and site clinical trial activities across study start-up or conduct and close-out, based on business needs and role scope.
The role interacts closely with local/regional clinical teams, internal Pfizer stakeholders,



investigator sites, and external partners to support smooth operational workflows in compliance with ICH/GCP, SOPs, and local regulatory requirements.
We are looking for hard-working, talented, high-caliber people. We know that employee satisfaction leads to customer satisfaction, which is the ultimate driver of long-term success.
As the company that conducts vital clinical studies for sponsors, including the world's leading biotech’s and top 50 pharmaceutical companies, we offer you enormous security and long-term prospects.
You will work from your home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.
JOB RESPONSIBILITIES
Country & Site Operational Support
Execute operational tasks across start-up, conduct and close-out phases.
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📌 GCO Associate I (España)
🏢 Parexel
📍 España