Director, Regulatory Advertising & Promotion

• Provide strategic leadership and oversight for compliance-focused regulatory review of promotional materials across media types, products, and therapeutic areas as assigned
• Establish and maintain a consistent, risk-based framework to ensure promotional content and materials comply with FDA regulations, including 21 CFR 202.1, FTC requirements, the PhRMA Code, internal policies, and other applicable laws
• Oversee timely and accurate submission of promotional materials to FDA, including Form FDA 2253 submissions and FDA Office of Prescription Drug Promotion (OPDP) advisory comment requests, as appropriate
• Build and maintain strategic relationships with regulatory authorities and represent the Company in relevant regulatory interactions related to advertising and promotion
• Lead identification, escalation, and resolution of promotional compliance risks, potential violations, deviations, and policy exceptions, partnering with Legal, Compliance, Commercial, Medical, and Regulatory stakeholders
• Direct audit and inspection readiness activities related to promotional and labeling compliance, ensuring appropriate documentation, governance evidence, and timely responses to requests

• Serve as a senior regulatory and compliance leader on the promotional review committee (MLR/PRC; PRC/SRC/MRC as applicable), providing strategic guidance, decision-making support, and alignment with internal policies and external compliance standards
• Lead development, implementation, and continuous improvement of SOPs, workflows, and controls used to develop, review, approve, and submit promotional materials
• Provide strategic input during early brand planning, campaign concept development, and copy development to enable compliant, efficient, and business-aligned MLR/PRC review and approval
• Develop and lead training for commercial and cross-functional teams on FDA advertising and promotion requirements, OPDP expectations, Subpart E, Form FDA 2253 submissions, and internal review standards as applicable
• Establish strong partnerships and governance practices with senior internal stakeholders to enable consistent interpretation, compliant execution, and timely decision-making
• Partner across Compliance & Legal to drive effective MLR/PRC governance, cross-functional alignment, issue resolution, and well-documented decisions
• Monitor evolving regulatory guidance, OPDP enforcement trends, industry practices, and relevant global considerations, and translate updates into actionable process, policy, and training enhancements

• Provide solution-oriented, innovative regulatory and compliance leadership that supports Company objectives while appropriately managing business, regulatory, and reputational risk
• Anticipate shifts in the regulatory environment and proactively advise leadership and business partners on potential impacts to promotional strategy, governance, and execution
• Incorporate diverse perspectives across the Company and externally to strengthen risk assessments, mitigation strategies, and decision quality
• Lead process improvement initiatives to increase the efficiency, consistency, and effectiveness of the advertising and promotion review function
• Provide leadership, coaching, and subject matter expertise to colleagues and cross-functional partners, contributing to team capability, knowledge sharing, and department development

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• Bachelor’s degree in a scientific discipline, pharmacy, public health, or a related field
• 10+ years of progressive experience in U.S. pharmaceutical/biotech compliance, regulatory affairs, or medical review focused on advertising and promotion, including significant experience in a senior review or governance leadership capacity
• Demonstrated experience leading or serving as a senior decision-making member of MLR/PRC for promotional and non-promotional materials
• Experience providing strategic, compliance-focused risk assessments and recommendations to senior cross-functional teams on promotional materials, campaigns, and activities for marketed products
• Deep working knowledge of FDA advertising and promotion requirements, including OPDP interactions, 21 CFR 202.1, Form FDA 2253 submissions, and Subpart E experience as applicable
• Familiarity with U.S. product labeling development and maintenance, and the connection between labeling and permissible promotional claims
• Experience maintaining documentation and audit readiness for promotional materials and labeling records, including supporting inspections and audits
• Proven ability to translate complex regulations into practical guidance, SOPs, workflows, controls, and governance models that enable timely, compliant execution at scale
• Strong executive presence, cross-functional influence, stakeholder management, and communication skills, with the ability to guide complex discussions and drive alignment among senior leaders
• Demonstrated judgment and integrity, with comfort identifying and escalating compliance risks, deviations, and policy exceptions
• Experience leading process improvement, governance, training, or inspection readiness initiatives within an advertising and promotion review function preferred

• Comprehensive medical coverage
• Dental and vision coverage
• Generous paid time-off
• 401(k) retirement plan with competitive company match
• Medical & Dependent Care Flexible Spending Account
• Up to $150 monthly cell phone reimbursement
• Employee Assistance Program
• Free parking

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.