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 wageLocal area$142.5k - $256.5k
The Associate Director, Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements for promotional... .... Guide promotional strategy as the Regulatory Ad Promo representative during early stages of product development...RegulatoryPermanent employmentWork at officeWork from home$148.5k - $214.5k
Job title: Associate Director, Global Medical Affairs - DermatologyLocation:Morristown, NJAbout the JobThe... ...emphasis on Atopic Dermatitis (AD), the early-stage dermatology pipeline... ...Commercial, Market Access, HEOR/RWE, Regulatory, Safety, Medical Communications, Publications...RegulatoryFull timeLocal area- 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
$171k - $210k
The Global Strategic Insights and Forecasting Partner is a key role within the Strategic... ...Commercial, Medical Affairs, Market Access, Regulatory, Finance, and R&D colleagues. Will be... ...appropriate, pro‑actively champion and deliver ad‑hoc market research projects to support...RegulatoryLocal area$154.4k - $242.55k
...will inspire you and empower you to shine? Join us as an Associate Director, Global Regulatory Project Management and Strategic Planning - Oncology TAU... .... TAUs & BUs) as appropriate, through both scheduled and ad‑hoc updates. Drive decision making processes and elevate...RegulatoryMinimum wageFull timeLocal areaRemote workWorldwide$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$154.4k - $242.55k
...company to inspire you and empower you to shine? Join us as an Associate Director, Global Biomarker Lead, Inflammation, GI2 TAU based in Cambridge,... ...documents, clinical protocols and documents submitted to Regulatory Agencies.• Establish and maintain scientific dialogue with...RegulatoryMinimum wageLocal area$154.4k - $242.55k
...strategic and tactical guidance to teams for the delivery of global regulatory strategies to support development and commercialization of... ...drafting and reviewing guidance comments and supporting trade association working groups.Education & Competencies (Technical and...RegulatoryMinimum wageLocal areaRemote work- ...Position Overview Bicara Therapeutics is seeking an Associate Director, Global Scientific Communications, who will lead the development and... ...strategic input from Clinical Development, Research, Biostats, Regulatory, Legal, and Corporate Communications. Tactical Delivery...RegulatoryWork at officeLocal area3 days per week
$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 wageLocal areaRemote workWorldwide- ...Ipsen seeks an Associate Director of Global Regulatory Affairs to develop and execute regulatory strategies for assigned biopharmaceutical programs. This role bridges R&D, commercial operations, and regulatory functions, ensuring compliant implementation across development...Regulatory
- Role: Global Strategic Insights and Forecasting Partner within the Strategic Business Excellence team, focusing on market analysis, forecasting... ...stakeholders including Commercial, Medical, Market Access, Regulatory, Finance, and R&D; support global and local decision-making,...RegulatoryLocal area
$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- Ipsen Biopharmaceuticals Inc. in Cambridge, MA, seeks an Associate Director, Global Regulatory Affairs to shape regulatory strategies for development and marketed products worldwide. You will guide regulatory asset teams and collaborate with R&D, Franchise, and Commercial...RegulatoryWorldwide
- Korro is seeking an Associate Director of Clinical Data Management in Cambridge, MA to lead data management for global studies, manage CRO relationships, and ensure regulatory-compliant, audit-ready data for submissions. The role partners with Clinical Development, Biostatistics...Regulatory
- Amylyx Pharmaceuticals, Inc. is seeking an Associate Director of Quality Control to lead commercial QC operations... .... The role emphasizes inspection readiness, global compliance, and collaboration across Manufacturing, Regulatory Affairs, and QA to ensure timely commercial...Regulatory
- Title: Associate Director, Global Regulatory Affairs Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid‑sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported...RegulatoryLocal areaWorldwide
$168k - $252k
...:The Modeling & Simulations Associate Director will be responsible for developing... ...in industry, academia or regulatory agencies.#LI-KM4At Vertex,... ...days per week on-site with ad hoc flexibility.Note: The Flex... ...InformationVertex is a global biotechnology company that invests...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week$157.6k - $236.4k
...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$174.4k - $261.6k
...DescriptionGeneral Summary:The RWE Associate Director is an integral member of the... ...knowledge of relevant RWE regulatory agency guidance and position... ...days per week on-site with ad hoc flexibility.Note: The... ...InformationVertex is a global biotechnology company that invests...RegulatoryFull timeSummer workRemote workFlexible hours2 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$156k - $234k
Job DescriptionRole SummaryThe AD, Source‑to‑Contract Process & Platform Enablement is... ...requirements and mitigate commercial and regulatory risk through execution.5. Supplier &... ...#LI-HybridCompany InformationVertex is a global biotechnology company that invests in scientific...RegulatoryFull timeContract workSummer workRemote workFlexible hours2 days per week$161.9k - $242.9k
...Job Description General Summary The Associate Director, Global Pain Forecasting & Analytics will join the Global Forecasting & Analytics team within... ...select 2. # On-Site: work five days per week on-site with ad hoc flexibility. Note: The Flex status for this...Summer workRemote workFlexible hoursShift work2 days per week$142.5k - $256.5k
The RoleModerna is looking for an Associate Director, Global Regulatory Affairs, CMC, to join our team. This pivotal role will focus on preparing and overseeing CMC and Quality related agency correspondence and regulatory applications, governing CMC submissions, and providing...RegulatoryPermanent employmentFull timeWork at officeWork from home$143k - $203k
...development and manufacturing) activities at global CRO/CMO sites, in alignment with program... ...studies in collaboration with internal AD/QC, QA teams and third parties.You will... ...completion of drug product sections of CMC-regulatory submission documents (IND, IMPD, NDA, PIP...Regulatory- ## Associate Director, HCP Experience – US PainApplylocations: Boston, MAtime... ...align with legal, regulatory, and compliance requirements... ...promotional programs in U.S. or global markets* Experience working... ...days per week on-site with ad hoc flexibility.Note: The Flex...RegulatorySummer workRemote workFlexible hours2 days per week
$211.57k - $250.7k
...people. We're proud to be a globally recognized top employer, wherean... ...employment. JOB TITLE: Associate Director, Biostatistics JOB DUTIES... ...with Clinical Development, Regulatory and Clinical Operations... ...analysis of trial data. Writes ADS and ad hoc analysis specifications...RegulatoryPermanent employmentWork at officeLocal area$160k - $240k
...Company Overview Rhythm is a global, commercial-stage... ...Overview Rhythm 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...RegulatoryInterim roleWork at office$144k - $216k
...Partner with clinical development, biometrics, regulatory, and study teams to develop and then... ...and regulatory Experience in a matrixed global organization spanning multiple sites and... ...interest, and ability to discern hype from true added value The annual base pay for this...RegulatoryFull timeTemporary workWork experience placement
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