Ann Marie Rahman Email & Phone Number | Develop global regulatory strategies to ensure timely submission and approval of CMC dossiers for commercial intermediates, drug substance and drug product (small molecule and biologics) for Clinical Trial and Marketing Applications. Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks. Educate stakeholders on intent and implications of CMC-specific regulations and guidance. Collaborate with International Affiliates, Manufacturing, Quality Assurance and Supply Chain to identify and establish appropriate risk-based solutions for projects. Serve as CMC regulatory representative with regulatory authorities for CMC meetings, including the planning and leading of meetings. Provide direct supervision of individuals including mentoring and performance management.

Ann Marie Rahman

Develop global regulatory strategies to ensure timely submission and approval of CMC dossiers for co...
North Chicago, Illinois, United States

*50 free lookup(s) per month.

Ann Marie Rahman’s Email ann.rahman@abbvie.com

Ann Marie Rahman’s Phone Numbers

Get ANN’s Phone Number (For Free)

Social Media

Ann Marie Rahman’s Location North Chicago, Illinois, United States

Ann Marie Rahman’s Current Industry Abbvie

Ann Marie Rahman’s Prior Industry Abbott Laboratories

Find accurate emails & phone numbers for over 700M professionals.

Director of Regulatory Affairs CMC

2021-02-01T00:00:00.000Z - Present

Associate Director- Regulatory Affairs CMC

2011-07-01T00:00:00.000Z - 2013-01-01T00:00:00.000Z

No Skills Available

No Languages Available

Ann Marie Rahman is a Develop global regulatory strategies to ensure timely submission and approval of CMC dossiers for commercial intermediates, drug substance and drug product (small molecule and biologics) for Clinical Trial and Marketing Applications. Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks. Educate stakeholders on intent and implications of CMC-specific regulations and guidance. Collaborate with International Affiliates, Manufacturing, Quality Assurance and Supply Chain to identify and establish appropriate risk-based solutions for projects. Serve as CMC regulatory representative with regulatory authorities for CMC meetings, including the planning and leading of meetings. Provide direct supervision of individuals including mentoring and performance management.