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
$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$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 areaRemote work- 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
$148.5k - $214.5k
Job title: Associate Director, Global Medical Affairs - Dermatology Location: Morristown, NJ About the... ...emphasis on Atopic Dermatitis (AD), the early-stage dermatology pipeline... ...Commercial, Market Access, HEOR/RWE, Regulatory, Safety, Medical Communications, Publications...RegulatoryLocal area$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
Job Description ACCOUNTABILITIES Partnering with the program Global Regulatory Lead (GRL), co-lead and facilitate product-specific Global Regulatory... .... TAUs & BUs) as appropriate, through both scheduled and ad-hoc updates. Drive decision making processes and elevate...RegulatoryMinimum wageFull timeWork at officeLocal areaRemote workWorldwide- ...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
- Takeda's Global Regulatory Affairs - CMC team in Cambridge, MA is seeking a Regulatory CMC professional to lead regulatory submissions for investigational, registration and post-approval programs across global markets. With minimal supervision, you will define CMC content...Regulatory
- ...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...RegulatoryFull timeLocal areaRemote work
$154.4k - $242.55k
...Represent Translational and Biomarker Research on Project and Global Product Teams to provide pharmacodynamic, disease and predictive... ...nomination documents, clinical protocols and documents submitted to Regulatory Agencies. Establish and maintain scientific dialogue with KOLs...RegulatoryMinimum wageFull timeLocal areaWorldwide- ...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...RegulatoryWorldwide
$154.4k - $242.55k
...Objective / Purpose: Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives... ...the field as applicable. Accountabilities: The Associate Director will be responsible for highly complex or multiple...RegulatoryMinimum wageFull timeLocal areaRemote work- 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
- Ipsen Biopharmaceuticals Inc. seeks an Associate Director, Global Regulatory Affairs to lead regulatory strategies for our portfolio, coordinating with R&D, Franchise, and Commercial teams. The role requires directing global regulatory activities, ensuring timely and compliant...Regulatory
- Clinical Dynamix, Inc. seeks an Associate Director, Clinical Operations to lead and optimize global trials from Watertown, MA. You will plan, execute, and oversee... ...sites, and vendor teams. Existing expertise in regulatory guidelines, cross-functional leadership, and fast...Regulatory
- Associate Director, Global Regulatory Affairs 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 by nearly...RegulatoryLocal areaWorldwide
$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$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- ...JOB TITLE: Associate Director (AD) – Case Management and Strategic Partnerships REPORTS TO: Vice... ...operations, and PV alliance management within Global PV Operations. The role leads clinical... ...ICSR processing activities meet regulatory requirements, established quality...RegulatoryFull time
$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...RegulatoryTemporary workLocal 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$159k - $195k
...experienced programmer to join us as Associate Director, Statistical Programming.... ...support clinical trials, regulatory submissions, and other key... ...Lead the execution of ad‑hoc and post‑hoc analyses to... ...with ICH/GCP guidelines and global regulatory submission requirements...RegulatoryFull timeContract workLocal areaFlexible hours3 days per week- Takeda Pharmaceutical Co. is seeking an Associate Director to translate scientific evidence into clear medical communications for neuroscience... ..., and manage content development with an emphasis on accuracy, balance, and regulatory #J-18808-Ljbffr Takeda Pharmaceutical Co.Regulatory
$161.5k - $218.5k
...Overview The Associate Director of Marketing, KOL Engagement and Enablement... ...Marketing, Medical Affairs, Global, Legal, Compliance, and field... ...priorities and regulatory requirements. Vendor & Agency... ...Experience building and leading ad boards, the TLL organization...RegulatoryFull timeTemporary workFlexible hours$153.9k - $230.9k
...and application of quality and regulatory compliance. The individual... ...responsibilities. This position reports to Director, GMP Operations Quality. This... ...days per week on-site with ad hoc flexibility.Note: The Flex... ...InformationVertex is a global biotechnology company that invests...RegulatoryFull timeWork experience placementSummer workWork at officeRemote workFlexible hours2 days per week3 days per week$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... ...of drug product sections of CMC-regulatory submission documents (IND, IMPD, NDA, PIP...Regulatory$150.84k - $226.26k
The Associate Director, Laboratory Space Planning is responsible for overseeing... ..., and applicable regulatory requirements. The role partners... ...planning and space discussions for global Oncology R&D managed sites,... ...efficiency. Working with AD Lab Insights to understand laboratory...RegulatoryTemporary workRelocation$155k - $225k
...critical unmet need. As a global leader in myostatin biology,... ...our team. The Senior Manager/Associate Director, Biostatistics will participate... ...from clinical design to regulatory submission. The Biostatistics... ...-specified analysis plan or ad-hoc analyses. Develop or review...Regulatory$154.4k - $242.55k
Program Management, Associate Director - Global Oncology Join Takeda as Program Management, Associate Director- Global Oncology out of Cambridge,... ...member of the OBU PMO, provide program management expertise and ad hoc project-based support for enterprise initiatives....Minimum wageFull timeCasual workWork at officeLocal areaRemote workWorldwide$204k - $306k
...Crinetics Pharmaceuticals on September 1 adding commercial and pipeline... ...Union and is under review by other global regulatory authorities. Atumelnant is an investigational... ...: The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical...RegulatoryFull timeSummer workRemote workFlexible hours2 days per week
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