Scorpion Therapeutics is hiring: Senior Director, Advertising and Promotion in N

Position Summary The Sr. Director, Advertising and Promotion is a strategic role leading the review and approval and submission of advertising and promotional materials, related training, and other nonproduct commercial communications. In this role, you will be responsible for ensuring compliance with regulatory agencies’ requirements and Invivyd’s promotional, medical, and corporate communications objectives. Responsibilities Represents Regulatory Affairs as a member of cross‑functional commercial review committee, providing regulatory input into the review and approval of promotional and nonpromotional materials Maintain a deep and current awareness of evolving US and global regulations, Codes and guidelines, enforcement actions and policy issues affecting the pharmaceutical/biotech Industry as it pertains to labeling and promotion Effectively partner and collaborate with Medical Affairs, Legal, Compliance, Commercial, and other stakeholders as needed to ensure that promotional and non‑promotional materials are reviewed in a timely fashion throughout the product life cycle Primary Liaison with OPDP and effectively manage relationships with FDA contacts Provide strategic regulatory advice for labeling taking into consideration marketing use post‑approval Interpret and communicate regulatory perspective on promotional and non‑promotional activities and risks to all stakeholders and management Coordinate regulatory training on regulatory issues pertaining to advertisement and promotion activities Requirements Doctorate, Master's, or Bachelor's degree in a relevant/scientific discipline (graduate degree preferred) Minimum of eight years working in the pharmaceutical or biotech industry with a minimum of 10‑15 years in Regulatory Affairs Experience working with OPDP Thorough knowledge of US regulatory requirements pertaining to marketing authorization filings for new products or updates to existing products particularly related to advertising and promotion Knowledge of global drug/biologic regulations and standards particularly related to promotion including but not limited to EU and international Requirements is a plus Ability to work in a fast-paced environment where drive is critical to success Ability to assess areas of regulatory risk and effectively communicate and coordinate discussions to influence all business functions in order to reach resolution Strong writing, project management and communication skills Ability to travel as needed (2x a month) to our New Haven, CT office Pay Range $220,000 - $293,000 The pay range represents the expected full‑time base salary for this role at the time of posting. At Invivyd we strive to create a welcoming and inclusive environment. Invivyd is proud to be an equal opportunity employer.