Director/Sr. Director Regulatory Labeling Strategy, Advertising, and Promotion, Regulatory
$183.55k - $275.32kKinsley Power Systems
Director/Sr. Director, Regulatory Labeling Strategy, Advertising, and Promotion, Regulatory Who we are: At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture – one that sparks bold thinking and strengthens our connections with each other and with the rare disease communities we serve. We embrace diverse backgrounds with respect, active listening, and a commitment to inclusion – because our differences shape how we hire, collaborate, and innovate. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities. Our commitment is more than scientific – it’s deeply personal, grounded in the meaningful connections we have built. To learn more, visit and follow Agios on LinkedIn and X. The impact you will make: Agios Pharmaceuticals is searching for a dynamic Director/Sr Director, Regulatory Labeling Strategy, Advertising, and Promotion to provide expert, strategic regulatory guidance and oversight for all labeling activities and promotional and non‑promotional communications to ensure compliance with applicable regulations, including FDA requirements. This individual will be responsible for development of global labeling documents (e.g. CCDS, regional product information, and patient leaflets) and serve on the Agios Review Committee as the Regulatory Reviewer responsible for the review and approval of promotional and non‑promotional materials across the Agios portfolio. This individual will partner cross‑functionally with Legal, Commercial, Corporate Communications, and Medical, as well as other cross‑functional stakeholders within the Research and Development organization, to enable compliant, effective messaging, development of labeling, and promotional and non‑promotional materials to support business objectives while protecting the company’s integrity and reputation. What you will do: Provide global regulatory labeling expertise and ensure adherence to global regulations in support of the development, review, and approval of labeling documents. Manage the creation and/or maintenance of global labeling strategy and documents (e.g. CCDS, regional product information, and patient leaflets). Collaborate closely with Commercial, Clinical, Legal, and Medical, as well as other cross‑functional stakeholders within research and development, to shape compliant messaging strategies and effective labeling documents. Lead regulatory strategy for advertising and promotional materials across all stages (pre‑approval, launch, and lifecycle) by serving on the Agios Review Committee (ARC) as the Regulatory Reviewer responsible for the review and approval of promotional and non‑promotional materials across the Agios portfolio. Serve as the internal subject matter expert on FDA advertising and promotion regulations, including OPDP expectations and evolving enforcement trends. Ensure timely and accurate FDA 2253 submissions of US promotional materials. Interface with regulatory authorities (e.g., OPDP) as needed, including managing inquiries or enforcement responses. Provide risk‑based guidance that balances compliance with business impact and speed. Ensure all materials (HCP, patient, digital, payer, investor‑facing where applicable) meet regulatory requirements. Guide teams on appropriate claim substantiation, fair balance, and risk disclosure. Regularly assess labeling updates to determine their impact on previously approved materials and identify when revisions are required, ensuring changes are reflected in current promotional and advertising materials. Influence brand planning, campaign development, and launch readiness. Act as a trusted advisor to senior leadership on promotional risk and opportunity. Develop and maintain internal policies, SOPs, and guidance related to labeling and promotional practices. Drive continuous improvement of review processes to enhance speed, clarity, and effectiveness. Implement scalable systems appropriate for a growing organization. Lead / oversee training programs for cross‑functional teams on labeling regulatory requirements and best practices. Foster a culture of compliant innovation and accountability. What you bring: Bachelor’s degree required; advanced degree (PhD, PharmD, JD, or MS) preferred. Director: 10+ years of experience in Regulatory Affairs within the biopharmaceutical industry. 7+ years experience developing regulatory labeling documents (CCDS, local labels, patient leaflets). 7+ years experience in Advertising & Promotion / OPDP compliance. Senior Director: 15+ years of experience in Regulatory Affairs within the biopharmaceutical industry. 12+ years experience developing regulatory labeling documents (CCDS, local labels, patient leaflets). 12+ years experience in Advertising & Promotion / OPDP compliance. Demonstrated experience leading Medical, Legal and Regulatory review processes. Strong knowledge of FDA regulations, guidance, and enforcement trends related to promotion. Proven ability to operate both strategically and tactically. Strong track record of cross‑functional influence, external engagement, and operating effectively in a matrixed environment with cross‑functional teams. Experience supporting late‑stage assets and/or product launches preferred. Concerned that you don’t check off every box in the requirements listed above? Please apply anyway! At Agios, we value each other’s differences and recognize that teams thrive when everyone brings their unique experiences to the table. We are dedicated to building an inclusive, diverse, equitable, and accessible environment where all employees can bring their whole selves to work. If you’re excited about this role but your previous experience doesn’t align perfectly with the job description, we still encourage you to apply. You may be just the right candidate for this role or another opening! Work Location: Location Agnostic: Work location for this role is based on employee’s individual preference. This role has the ability to be either remote in the US or hybrid in our Cambridge Headquarters. Hybrid schedules vary but are generally less than 3 days per week onsite and hybrid employees are expected to live within commutable distance to our Cambridge Headquarters. Remote employees work entirely from home except for attending company‑sponsored events/meetings. For employees who choose to work remotely, travel may be required for certain company events commensurate to the above job description. What we will give you: Deliberate Development. Your professional growth as one of our top priorities. Flexibility. We’re all about individual needs. We embrace different perspectives, work styles, health and wellness approaches, care of families and productivity. When you’re at your best, we’re at our best. Premium benefits package. We invest in the health, wellbeing, and security of our people with a premium benefits package that is well‑rounded and flexible to help meet the varied personal and professional needs of every member of our team. For more detail on the benefits we offer at Agios, visit the Inside Agios section of our website. Competitive and equitable performance‑based compensation. This includes base salary and both short‑ and long‑term incentives that are connected to our business strategy and vary based on individual and company performance. The current base salary range for this position at the Director level is expected to be between $183,549 and $275,324 annualized and the current base salary range for this position at the Senior Director level is expected to be between $229,562 and $344,342 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Psychological safety. We support an environment of fearlessness. We want you to share your ideas, speak candidly and take data‑informed risks to help push the boundaries. Commitment to diversity. We strive to foster a welcoming workplace where everyone can thrive. We’re continuously looking to improve the inclusivity of our workforce. Commitment to community. We’re an active participant in the communities that surround us – the communities where we live, and the community of people and their loved ones in need of better treatment options for conditions that are often overlooked. Interested in learning more about what makes our culture unique? Visit the Inside Agios section of our website. #J-18808-Ljbffr
$238k - $294k
...challenge with radical care. Position Description The Sr. Director, Regulatory Labeling, Advertising & Promotion (LAP) is responsible for leading global product... ...and Safety, and plays a central role in labeling strategy, lifecycle management, and promotional material...SeniorFull timeWork at officeFlexible hours3 days per week$235k - $260k
...seeking an experienced and strategic Senior Director of Regulatory Affairs Advertising/Promotion to lead FDA-focused promotional regulatory strategy for a fast-paced pharmaceutical startup... ..., stakeholders, and teams and lead labeling activities. The Senior Director...SeniorWork at office- ...Agios Pharmaceuticals seeks a Director/Sr. Director for Regulatory Labeling Strategy to provide strategic regulatory guidance. You will oversee labeling activities... ..., and Medical teams, as well as reviewing promotional materials. The ideal candidate possesses significant...SuggestedRemote work
$193.18k - $236.1k
...How You Will Achieve More: The Associate Director, Regulatory Affairs Advertising, Promotion & Labeling (AD RA-APL) provides regulatory advertising and promotion... ...strategic objectives and commercial regulatory strategy. Develops innovative and compliant...SuggestedWork at officeRemote work$178.5k - $257.83k
Mass Digital Health is seeking a Director for US Advertising and Promotion in Global Regulatory Affairs. This role entails providing strategic direction and oversight... ...of assigned products, developing regulatory strategies, and mentoring a team within a supportive environment...Suggested$130k - $190k
...Manager/Senior Manager Regulatory Affairs – Advertising, Labeling, and Promotion Cambridge, MA Added 2/13/2026 Company Overview... ...range of therapeutic editing strategies that Beam is using to advance a... .... This role reports to the Director of Regulatory Labeling and serves...Senior$178.5k - $257.83k
## Director, US Regulatory Affairs - Advertising and PromotionBewerbenlocations: Morristown... ...- Advertising and Promotion (Hybrid)**Location:... ...with the Sr. Director/Product Support... ...regulatory strategies for marketed products... ...global organization for labeling strategies of...$200k - $300k
...ScholarRock and on LinkedIn. Summary of Position The Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs... ...(e.g., SOPs, business development, clinical labeling, disclosure) as needed Candidate Requirements Education...SeniorWork at officeLocal areaShift work- ...boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Director, Global Regulatory Labeling Strategy where you will be responsible for the development and implementation of labeling content and strategy of...Local areaImmediate startWorldwide
$130k - $190k
...biotechnology company in Cambridge is seeking a Manager/Senior Manager for Regulatory Affairs focusing on Advertising, Labeling, and Promotion. This role involves leading U.S. promotional regulatory strategy, overseeing compliance for promotional materials, and managing...$187.5k - $275k
...medicines for serious diseases. Regulatory affairs collaborates cross... ...successful regulatory strategies. Verve is located in Boston,... ...Responsibilities The Senior Director, Regulatory Affairs is responsible... ...the details of any promotion or transfer of Lilly employees...SeniorFull timeWork at officeFlexible hours3 days per week- ...X-TOLE3, which would support regulatory submissions outside the U.S.,... ...About the Role We are seeking a Director, Regulatory Affairs, Commercial (Advertising & Promotion), to join our Regulatory Affairs... ...regulatory and brand strategy. The Director will have oversight...Temporary workWork at office2 days per week
- ...A leading BioPharmaceutical company seeks a Senior Director, Global Regulatory Strategy, to lead regulatory efforts for early-stage products and ensure alignment with health authority expectations. The role demands extensive regulatory experience in the pharmaceutical...Senior
- ...Associate Director, Global Regulatory Affairs, Advertising and Promotion Job Description At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients worldwide. The Associate Director, Global...Full timeRemote workWorldwide
$209.35k - $258.6k
Director, Regulatory Labeling Regulatory Affairs Cambridge, MA * ID: 26R-19 * Full-Time/Regular This position is currently based... ...responsible for shaping and executing global labeling strategy across Akebia's portfolio. This individual will serve as...Work at officeLocal areaRelocationFlexible hours$187.5k - $275k
...Eli Lilly and Company is seeking a Senior Director of Regulatory Strategy in Boston, MA. This role involves leading the planning and implementation of regulatory strategies for gene-editing programs, managing submissions, and ensuring compliance with regulatory standards...Senior$270k - $330k
...Position Overview The Senior Director, Global Regulatory Affairs, Oncology is... ...flawless execution of regulatory strategies for both development and... ...objectives. Define optimal label, sequencing indications, dosage... ..., train, compensate, and promote without regard to an individual...SeniorTemporary workWorldwideFlexible hours$270k - $330k
...The Senior Director, Global Regulatory Affairs, Oncology is accountable for providing... ...execution of regulatory strategies for assigned products and projects... ...impact on timelines and/or label; propose remediation where... ..., train, compensate, and promote without regard to an...SeniorTemporary workLocal areaWorldwideFlexible hours$122.25k - $176.58k
**Job Title:** Senior Manager, Regulatory Affairs Advertising and Promotion**Location:** Morristown, NJ**/**Cambridge... ...develop and implement regulatory strategies for promotion and advertising... ...implementation of regulatory strategies for labeling, product defense, and development...SeniorWork experience placement$211.85k - $317.78k
...Job Title: Senior Director, Global Regulatory Strategy - Early Development & Business Development Location: Boston, MA At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately...SeniorHourly payTemporary workWork at office3 days per week$115 - $125 per hour
...Job Description The Regulatory Strategy Director will be responsible for the development and implementation of innovative global/regional regulatory... ...recommendations. Experience with market product, labeling, new drug development and working with the FDA is required...Contract workLocal area- ...Regulatory Strategy Senior Director page is loaded## Regulatory Strategy Senior Directorlocations: Boston, MAtime type: Full timeposted on: Posted... ...analyzing and interpreting data, protocols, safety reporting, labeling and other activities related to the phases of drug...SeniorSummer workLocal areaRemote workFlexible hours2 days per week3 days per week
$178.5k - $257.83k
...Job Title Director, US Advertising and Promotion, Global Regulatory Affairs Location Morristown, NJ / Cambridge, MA Job Summary In this... ...and Promotion (A&P) group on promotion, labeling, product defense, and development strategies for assigned product(s). The Director is...- Director, Regulatory Affairs Advertising & Promotion Position Summary We are seeking a highly experienced and strategic Director, Regulatory Affairs Advertising... ...will play a critical role in shaping promotional strategy, guiding cross-functional teams through complex...Work at office
- ...Job Description The Director Regulatory Affairs Global Regulatory Lead... ...GRL I) in Global Regulatory Strategy is responsible for developing... .../Canada) role. May lead the Labeling Regulatory Strategy Team (LRST... ...regulatory strategies with Sr. Management Under direction...Temporary workLocal areaWorldwide
$157.08k - $239.7k
...Overview The Associate Director, Regulatory, within the... ...and governance for promotional materials across media... ...to promotional and labeling compliance, including... ...commercial teams on FDA advertising and promotion... ...assessments and mitigation strategies Identify and...Fixed term contractWork at officeFlexible hours3 days per week- ...A leading biotechnology company in Boston is seeking a Regulatory Strategy Senior Director to oversee global regulatory strategies for development programs. The role involves leading regulatory strategy development, ensuring cohesive integration of regulatory ideas, and...Senior3 days per week
- ...Sanofi in Cambridge, MA is hiring a Director for US Advertising and Promotion in Global Regulatory Affairs. This role is pivotal in overseeing strategies and decision-making for assigned products and ensuring compliance with regulations. The ideal candidate should have...
- ...Sanofi is looking for a Director of US Regulatory Affairs - Advertising and Promotion to join our team in Cambridge, MA or Morristown, NJ. This hybrid role involves ensuring compliance of promotional materials with US regulations and mentoring team members. The ideal candidate...
$209.35k - $258.6k
...Akebia Therapeutics(R), Inc. in Cambridge, MA is seeking a Director of Regulatory Affairs – Labeling. This leadership role will shape global labeling strategies for the product portfolio. Candidates should have over 10 years in regulatory labeling within pharmaceuticals...
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