Location
Remote, Turkey, Turkey
Posted
June 20, 2026
Job Description
Site Activation Partner
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
+ Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for s...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
+ Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for s...