Regulatory Affairs Specialist

An experienced Regulatory Affairs Specialist is needed to ensure compliance with national and international regulations for clinical trial submissions and approvals.

Key Responsibilities:

• Prepare, review, and submit regulatory documents (e.g., CTAs, amendments).
• Liaise effectively with regulatory authorities (e.g., DCGI, Ethics Committees).
• Monitor and interpret changes in regulatory guidelines and ensure compliance.
• Provide regulatory guidance to internal teams and clients.

Experience Required:

• 3-5 Years Exp.