Regulatory Affairs Specialist

3 days ago


Fatih, Istanbul, Turkey Syneos Health, Inc. Full time

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Syneos Health, Inc. In this role, you will be responsible for ensuring the quality of deliverables at the country level, following project requirements and applicable country rules.

The successful candidate will have excellent understanding of clinical trial process across Phases II-IV and ICH GCP, with strong organizational skills and ability to handle multiple projects. They will be responsible for monitoring financial aspects of the project and the number of hours/tasks available per contract, escalating discrepancies in a timely fashion.

In this role, you will work closely with the SSU Country Manager to ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements. You will also review and comply with Standard Operating Procedures (SOPs) and Work Instructions (WI) in a timely manner, keeping training records updated accordingly.

We offer a dynamic and collaborative work environment where you can grow and develop your career. If you are passionate about delivering high-quality results and making a difference in the lives of patients, we encourage you to apply for this exciting opportunity.



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