Global Regulatory Affairs Associate

Job Summary

A company is looking for an Associate/Sr. Associate/Manager in Global Regulatory Affairs focused on Regulatory Delivery & Excellence.

Key Responsibilities

• Lead the registration management process, ensuring compliance with submission regulations and technical content
• Develop collaborative relationships with cross-functional teams to influence electronic registration plans and strategies
• Own the registration management process at the molecule/project level, ensuring timely and accurate electronic records

Required Qualifications

• BS in a technical or scientific discipline (e.g., chemistry, biology, pharmacy)
• 2+ years of experience with the drug development process
• Previous project management and global submission experience preferred
• Demonstrated ability to operate in a highly regulated environment
• Knowledge of drug development processes and regulatory strategies