Associate Director Clinical Regulatory

Job Summary

A company is looking for an Associate Director, Global Clinical Regulatory Lead.

Key Responsibilities

• Provide strategic and operational direction for regulatory activities related to drug products
• Oversee IND submissions and clinical trial applications, ensuring compliance with regulations
• Collaborate with cross-functional teams and external stakeholders to support product registrations

Required Qualifications

• Bachelor's degree in a life science field with a minimum of 5 years of experience in the Pharma/Bio Industry, or an MS, PhD, or PharmD with 4-5 years of experience in Regulatory Affairs
• Knowledge of regional regulatory guidelines and experience managing clinical trial applications
• Demonstrated experience in building stakeholder relationships with cross-functional teams
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel up to 5% as required