Global Regulatory Ad & Promo Associate Director
Moderna Therapeutics
Moderna is seeking an Associate Director, Global Regulatory Advertising and Promotion to ensure FDA and global promotional compliance across channels. You will serve as a liaison among Regulatory Affairs, Legal, Medical, and Commercial teams to align regulatory strategy with business goals. The role requires 5+ years in regulatory affairs with a focus on advertising and promotion, experience with PMRT/MRC, and familiarity with EMA, Health Canada, and UK authorities. #J-18808-Ljbffr Moderna Therapeutics
$154.4k - $242.55k
...Pharmaceutical Sciences and Precision MedicineThe Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU)... ...in the biopharmaceutical industry (e.g., safety, ad promo, regulatory strategy, medical affairs, etc.). 5-7...RegulatoryMinimum wageTemporary workLocal area$142.5k - $256.5k
The Role The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements... .... Guide promotional strategy as the Regulatory Ad Promo representative during early stages of product development...RegulatoryWork at officeWork from home$152k - $209k
...member of myGwork – the largest global platform for the LGBTQ+ business... ...in neuroscience. The role of the Associate Director requires the ability to provide regulatory strategic advice primarily for U... ...franchises Assist Regulatory Ad Promo department in monitoring...RegulatoryFull timeTemporary workWork at officeLocal area$142.5k - $256.5k
The Role The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements... .... Guide promotional strategy as the Regulatory Ad Promo representative during early stages of product development...RegulatoryPermanent employmentWork at officeWork from home$163.2k - $244.8k
Job DescriptionGeneral Summary:The Associate Director, Global Submission Management (GSM) is responsible... ...execution of a portfolio of global regulatory submissions across development and lifecycle... ...work five days per week on-site with ad hoc flexibility.Note: The Flex status...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week- Moderna is seeking an Associate Director for Global Regulatory Advertising and Promotion to ensure regulatory compliance across promotional materials and communications. You will collaborate with Regulatory Affairs, Legal, Medical, and Commercial teams to guide advertising...Regulatory
- Moderna is seeking an Associate Director, Global Regulatory Advertising and Promotion to ensure FDA and global promotional materials comply with regulatory requirements across channels. You will liaison with Regulatory Affairs, Legal, Medical, and Commercial teams, guiding...Regulatory
- Moderna seeks an Associate Director, Global Regulatory Advertising and Promotion to ensure compliance across promotional and non-promotional materials. You will liaise with Regulatory Affairs, Legal, Medical, and Commercial teams to provide strategic guidance on advertising...Regulatory
$154.4k - $242.55k
...is to accelerate access to transformative medicines and make a lasting impact on patients worldwide.Join Takeda as Associate Director, Global Regulatory Lead Oncology where you will be part of the global regulatory team. As Associate Director, Global Regulatory Lead Oncology...RegulatoryMinimum wageLocal areaRemote workWorldwide$183k - $252k
About the RoleThe Global Associate Medical Director, Evidence Generation and Education is a key member of the Global Medical Rare Disease team, reporting... ...Economics and Outcomes Research, Value and Access, Regulatory, Patient Advocacy, Regional Medical, Commercial,...RegulatoryFull timeTemporary workLocal areaWorldwide$154.4k - $242.55k
...push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of...RegulatoryMinimum wageTemporary workLocal areaRemote workWorldwide$135k - $225k
...reimbursement, product commercialization, and regulatory and compliance solutions. Do you think... ...our communities.What You Will Do:The Global Market Access team provides... ...across major and emerging global markets.Associate Directors are key members of the Global Market Access...RegulatoryFull timeWork experience placementImmediate startRemote workFlexible hours$169.4k - $266.2k
...empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Director, Global Scientific Communications Group Lead. This... ...including ideas for sub-analysesCompliance and Regulatory: Excellent understanding of regulatory,...RegulatoryMinimum wageTemporary workFor contractorsFreelanceLocal areaRemote work$150k - $200k
...The Associate Director, Advertising and Promotion Compliance, US will serve as the Regulatory Affairs (RA) representative for assigned products... ...primary liaison with FDA on ad/promo regulatory issues concerning... ...for ensuring adherence to global compliance standards and FDA...RegulatoryTemporary workWork at officeFlexible hours3 days per week- ...leading biotech company in Cambridge, MA, seeks an experienced Associate Director of Regulatory Strategy to lead oncology therapeutic programs. This role... ...in oncology, to ensure alignment between US and global strategies. Exceptional communication skills and leadership...Regulatory
- Scorpion Therapeutics in Cambridge, MA is seeking a Global Regulatory Labeling Strategy Lead (Associate Director) for the Plasma-Derived Therapies Business Unit. You will drive labeling strategy for US/EU, CCDS maintenance, and cross-functional program leadership. Hybrid...Regulatory
- Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) Responsibilities: Provide regulatory expertise and strategic guidance to internal stakeholders to develop and maintain pharmaceutical drug/device labeling. Contribute...Regulatory
$155k - $214k
About This Role:As the Associate Director, Global Quality Risk Management, you will be at the forefront of Biogen’s commitment to quality excellence... ..., your role is pivotal in aligning with ICH Q9 and global regulatory expectations. Reporting to the Director of Quality Risk...RegulatoryFull timeTemporary workLocal area- Overview Moderna Therapeutics is seeking an Associate Director of Regulatory Strategy to support programs within the oncology franchise in one of Moderna... ...based on messenger RNA technology in the US and other global markets. Responsibilities Serve as the global...Regulatory
- 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...RegulatoryFull timeRemote workWorldwide
$190k - $210k
...breast cancer treatment paradigm and access a $15 billion global market opportunity. Our follow‑on product candidate, OP... ...your career, and for what’s beyond . About the Role Associate Director, Global Regulatory Affairs, Compliance As the Global Associate Director, Regulatory...RegulatoryWork at officeFlexible hours2 days per week$90k - $115k
Associate Director, Global Quality (R&D) Pay Range: $90,000.00 - $115,000.00 per year Travel may be required. We are partnered with a biotechnology... ..., this role ensures alignment with international regulatory standards while driving inspection readiness, vendor oversight...RegulatoryWork experience placementRemote workWorldwideShift work- ...Associate Director, Global Investment Legal Services – Attorney MIT Investment Management Company (“MITIMCo”) is the department within MIT... ...investments in emerging managers, including evaluating non-U.S. regulatory requirements and sourcing and maintaining relationships...RegulatoryPermanent employmentFull timePart timeInternshipWork at office2 days per week
- ...:The Modeling & Simulations Associate Director will be responsible for developing... ...in industry, academia or regulatory agencies.#LI-KM4Pay Range:$1... ...days per week on-site with ad hoc flexibility.Note: The... ...HybridCompany InformationVertex is a global biotechnology company that...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week
$160k - $240k
Company OverviewRhythm is a global, commercial-stage biopharmaceutical... ...is seeking an Associate Director, Biostatistics to join our Biostatistics... ...partnering across clinical, regulatory, safety, data management,... ...analyses, DSMB meetings, ad hoc analyses, and other statistical...RegulatoryInterim roleWork at office- ...education grants and sponsorships within Global Medical.Ensures that funding decisions... ...transparency, efficiency and consistency without adding unnecessary bureaucracy.Provide... ...or markets with varied maturity levels, regulatory environments and industry‑code expectations...RegulatoryWork at officeLocal area
$185.3k - $250.7k
The Associate Director, Biostatistics is responsible for statistical activities... ...with Clinical Development, Regulatory and Clinical Operations... ...analysis of trial data.· Writes ADS and ad hoc analysis... ...people. We're proud to be a globally recognized top employer, where...RegulatoryFull timeTemporary workLocal areaFlexible hours- ...DescriptionGeneral Summary:The Associate Director, Medical Writing Science... ...for document development for regulatory filings and coordinates the... ...days per week on-site with ad hoc flexibility.Note: The Flex... ...HybridCompany InformationVertex is a global biotechnology company that...RegulatoryFull timeWork experience placementSummer workWork at officeRemote workRelocation packageFlexible hours2 days per week3 days per week
$166.4k - $249.6k
...Summary:The Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and commercial... ...select2. On-Site: work five days per week on-site with ad hoc flexibility.Note: The Flex status for this...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week$142.5k - $256.5k
The Role:The Associate Director, Global Regulatory-CMC will be responsible for coordinating regulatory CMC activities for one or more products, depending on complexity, through all stages of a products lifecycle. The Associate Director will be responsible for developing...RegulatoryPermanent employmentFull timeWork at officeWork from home
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