Senior Manager, Regulatory CMC Small Molecule Lead

at  Biogen

Job Description

ABOUT THE ROLE

In this role you are responsible for providing Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include preparation and compilation of submission/documentation for specific small molecule projects working as or working with the Regulatory CMC Lead and key stakeholders, primary contact for affiliates on Regulatory CMC activities in the assigned regions and managing of routine and non-routine Health Authority interactions as delegated. Depending on the stage of development and complexity of the program, this role can be a Regulatory CMC Lead for early stage development programs or working with the Regulatory CMC Lead for late stage development or commercial programs. The Regulatory CMC Lead is the primary global contact for Regulatory CMC activities associated with the program and will report to the Regulatory CMC Small Molecule Team Lead. This candidate must have proven leadership and abilities to work cross-functionally and across cultures. Strong communication, Regulatory CMC small molecule strategic and operational knowledge and interpersonal skills are required.

WHAT YOU’LL DO

• Providing strategic and operational Regulatory CMC expertise and support in cross-functional teams, as required, and working flexibly within and across regions to provide broad operational support to ensure the delivery of project/products and business objectives.
• Preparation and delivery of CMC Regulatory operational plans for products in the assigned regions and supporting the preparation and delivery of regulatory submissions (including IND/IMPD/CTAs/MAAs)
• Responsible for submission from defining content to leading reviews as required to ensure complete, concise and accurate submissions to Health Authorities. Writing and / or Review of regional and global CMC submission documents and responses to Health Authority questions
• Monitoring changes in the Regulatory CMC environment to support and advise key stakeholders and teams. Providing input into Regulatory CMC risks assessment and mitigation plans and ensuring they remain in line with the overall global Regulatory CMC strategy.
• Coordinating and completing regulatory assessments of CMC changes in the designated systems. Responsible for assuming responsibilities from the Team Lead or Global Regulatory CMC lead, as agreed and delegated, and maintaining open lines of communication on assigned projects/products to ensure awareness on status and issues relating to submissions. Responsible for leading or assisting in delivery of project assignments supporting business needs e.g. representation of Regulatory CMC on cross functional work streams. Responsible for leading or assisting in delivery of Regulatory CMC initiatives and the development of Regulatory CMC standards and SOPs, as assigned. Ensure that appropriate records are maintained in the designated system for submission in assigned regions