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Biogen
Associate Director Advertising and Promotion, Global Regulatory Affairs
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Based on Massachusetts data
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What they do
A Regulatory Affairs Manager plans, directs, or coordinates production activities of an organization to ensure compliance with regulations and standard operating procedures.
$225,694 / year median in Massachusetts
+1% projected growth
Job Description
At Biogen, we are pioneers in neuroscience. The role of the Associate Director requires the ability to provide regulatory strategic advice primarily for U.S. communications related to disease education, promotional materials and medical/scientific materials for healthcare providers, payors and patients in support of Biogen business objectives. The role may also require review of global, corporate, clinical trial, and pipeline materials and communications. This individual will effectively partner and collaborate with cross-functional stakeholders and ensure that materials are competitive and compliant with applicable FDA regulations and guidances, PhRMA guidelines, and Biogen policies. What You'll Do Provide regulatory strategic input, risk assessment, and mitigation strategies to various global and U.S. internal teams on branded and unbranded concepts, promotional materials, disease awareness communications, medical communications and sales training/education materials Provide strategic input on promotional claims implications to various global and U.S. internal teams responsible for late-stage clinical development plans Provide creative and solution-oriented feedback to meet business goals and further business objectives Serve as the primary point of contact with the Office of Prescription Drug Promotion (OPDP) for designated product(s) Provide strategic advice for the development of Advisory Comments submissions Ensure promotional materials are consistent with FDA-approved labeling, compliant with applicable FDA regulations, and completed in accordance with 2253 submission requirements Develop and maintain strong working relationships with internal colleagues including, but not limited to: Commercial, Medical, Legal, Compliance, Regulatory Strategy and Labeling, and Medical/Marketing Operations Work with management and Reg AP team members to ensure communications and feedback are generally consistent across franchises Assist Regulatory Ad Promo department in monitoring evolving regulatory landscape and communicating updates to internal stakeholders Who You Are Positive individual who demonstrates integrity and agility while working in fast-paced and compliant environment to advance external HCP, payor, and patient initiatives. Consistently manages and prioritizes multiple and competing responsibilities for an expanding business that strives to meaningfully change the lives of people living with serious neurological diseases. Required Skills BS required; advanced degree preferred Minimum of 4-5 years of Regulatory promotional review Detail and deadline oriented; well organized Capability to analyze and assess risk and then effectively communicate across interdisciplinary teams Ability to dissect and interpret complex disease information and product efficacy/safety data Demonstrates strong negotiation and interpersonal skills to influence others and build team collaboration, consensus and partnerships Adapts to dynamic environment and business needs Ability to develop and maintain relationships with OPDP Excellent verbal, written, and presentation skills