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Regulatory Affairs Specialist II
3 months ago
Position Overview:
As a Site Start-Up & Regulatory Specialist II at Syneos Health, you will play a crucial role in our biopharmaceutical solutions organization, which is dedicated to enhancing client success.
Key Responsibilities:
Your primary responsibilities will include:
- Facilitating the initiation of clinical trials by managing regulatory submissions and approvals.
- Collaborating with cross-functional teams to ensure compliance with industry regulations.
- Providing expert guidance on regulatory requirements and processes.
About Syneos Health:
We are committed to translating unique clinical, medical affairs, and commercial insights into actionable outcomes that meet the demands of the evolving market landscape.
