A company is looking for an Associate Director, CMC Regulatory Strategy.
Key Responsibilities
Lead the planning, authoring, and review of regulatory submissions for various projects
Provide in-depth reviews of protocols, reports, and documents for CMC Development or Commercial teams
Manage preparation and submission of responses to regulatory agencies and ensure compliance with regulatory strategies
Required Qualifications, Training, and Education
BSc / BA with experience in regulatory CMC or related fields
Demonstrated knowledge of CMC regulatory and drug lifecycle regulations
Experience with electronic Common Technical Document CMC regulatory documents
Understanding of FDA, EMA, and ICH guidelines
Exceptional interpersonal skills and ability to influence functional practices
Associate Director Cmc Regulatory • Newark, Delaware, United States