Current jobs related to Director, Global Medical Affairs - Cambridge, Massachusetts - Moderna, Inc.
-
Director of Dermatology Medical Affairs
23 hours ago
Cambridge, Massachusetts, United States Takeda Full timeAbout the RoleWe are seeking a highly skilled and experienced Director of Dermatology Medical Affairs to join our team at Takeda. As a key member of our US Medical Affairs organization, you will be responsible for developing and executing medical strategies for our dermatology products.Key ResponsibilitiesDevelop and execute medical strategies for assigned...
-
Global Medical Communications Director
5 days ago
Cambridge, Massachusetts, United States AAPC Full timeAbout the RoleWe are seeking a highly skilled Associate Director, Global Medical Communications to join our team. As a key member of our Global Medical Affairs department, you will play a critical role in developing and executing medical communication strategies across various disease areas.Key ResponsibilitiesDevelop and implement global medical...
-
Global Medical Communications Director
5 days ago
Cambridge, Massachusetts, United States AAPC Full timeAbout the RoleThe Associate Director, Global Medical Communications is a strategic role within Global Medical Affairs that collaborates with cross-functional partners to oversee one or more disease areas/assets on a Global level.Key ResponsibilitiesDevelop and execute medical communication plans encompassing tactics such as core content, scientific...
-
Director, Global Regulatory Affairs
2 weeks ago
Cambridge, Massachusetts, United States GlaxoSmithKline Full timeAbout the RoleWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at GlaxoSmithKline. As a key member of our Global Regulatory Affairs team, you will play a critical role in shaping our regulatory strategy and ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory...
-
Global Head of Regulatory Affairs
3 weeks ago
Cambridge, Massachusetts, United States Takeda Full timeWe invite you to become a part of our esteemed pharmaceutical organization as a Senior Director of Global Regulatory Affairs for Pharmaceuticals. In this pivotal role, you will be instrumental in formulating and executing comprehensive regulatory strategies for pharmaceutical products throughout their lifecycle, from development to market launch. Your...
-
Head of Global Public Affairs
1 day ago
Cambridge, Massachusetts, United States Takeda Full timeAbout the Role:Takeda, a patient-focused, values-based, R&D-driven global biopharmaceutical company, seeks a seasoned professional to lead its Multilateral Affairs team in Global Public Affairs. As a critical pillar of Global Corporate Affairs, this role is responsible for developing and executing Takeda's multilateral engagement strategy, optimizing...
-
Director, Regulatory Affairs CMC
5 days ago
Cambridge, Massachusetts, United States Takeda Full timeRegulatory Affairs Director, Small MoleculesTakeda is seeking a highly experienced Regulatory Affairs Director, Small Molecules to lead our Global Regulatory Affairs CMC team. As a key member of our team, you will be responsible for overseeing the development and execution of regulatory CMC development and registration strategies.Key Responsibilities:Plan,...
-
Global Public Affairs Leader
4 days ago
Cambridge, Massachusetts, United States Takeda Full timeAbout the Role:Takeda, a patient-focused, values-based, R&D-driven global biopharmaceutical company, seeks a seasoned professional to lead its Global Public Affairs team. As Head of Multilateral Affairs, you will be responsible for developing and executing Takeda's multilateral engagement strategy, optimizing international trade association engagement, and...
-
Senior Director of Regulatory Affairs
9 hours ago
Cambridge, Massachusetts, United States Apnimed Full timeJob Title: Senior Director, Regulatory AffairsApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly experienced Senior Director of Regulatory Affairs to play a key role in advancing our innovative programs through clinical trials and commercialization globally.Key...
-
Senior Director of Regulatory Affairs
7 days ago
Cambridge, Massachusetts, United States Apnimed Full time{"title": "Senior Director of Regulatory Affairs", "content": "Job SummaryApnimed is seeking a highly experienced Senior Director of Regulatory Affairs to lead the development and execution of regulatory strategies to support the approval and commercialization of our therapies globally.This is a key role in advancing our innovative programs through clinical...
-
Cambridge, Massachusetts, United States Takeda Full timeAbout the Role:The Associate Director, Global Medical Communications is a dynamic, strategic role within Global Medical Affairs that collaborates with cross-functional partners to oversee one or more disease areas/assets on a Global level. Responsible for the strategic co-development and execution of medical communication plans encompassing tactics such...
-
Cambridge, Massachusetts, United States Moderna Therapeutics Full timeAbout the RoleWe are seeking a highly experienced Regulatory Affairs Director to lead our medical devices, molecular testing, and biomarkers regulatory strategy and oversight. As a key member of our team, you will be responsible for ensuring that our products meet the highest regulatory standards and are compliant with global regulations.Key...
-
Cambridge, Massachusetts, United States AAPC Full timeJob SummaryWe are seeking an experienced Associate Director, Global Medical Information to join our team at AAPC. This individual will be responsible for providing timely, evidence-based, and fair-balanced medical information to external customers and internal stakeholders.Key ResponsibilitiesAdvance Medical Information Business Processes: Develop and...
-
Cambridge, Massachusetts, United States Apnimed Full timeAbout the RoleWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will play a critical role in advancing our innovative sleep apnea treatments through clinical trials and commercialization globally.Key ResponsibilitiesRegulatory Strategy and Planning:...
-
Cambridge, Massachusetts, United States AAPC Full time{"Job Title": "Associate Director, Medical Affairs, Adult Cholestatic Diseases", "Job Summary": "We are seeking a highly skilled Associate Director to join our Medical Affairs team in Cambridge, MA. As a key member of our team, you will be responsible for contributing to the medical strategies and overall US medical affairs plan for adult cholestatic...
-
Cambridge, Massachusetts, United States Apnimed Full timeJob SummaryWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will be responsible for developing and executing regulatory strategies to support the approval and commercialization of our therapies globally.Key ResponsibilitiesRegulatory Strategy and...
-
Director of Regulatory Affairs and Quality
2 weeks ago
Cambridge, Massachusetts, United States Philips Full timeJob SummaryWe are seeking a highly experienced and skilled Director of Regulatory Affairs and Quality to lead our Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities.Key ResponsibilitiesRegulatory Affairs Strategy and ExecutionDevelop and execute end-to-end regulatory...
-
Senior Director of Clinical Affairs
2 weeks ago
Cambridge, Massachusetts, United States Philips Full timeJob TitleSenior Director of Clinical AffairsJob SummaryWe are seeking a highly experienced and skilled Senior Director of Clinical Affairs to join our team at Philips. As a key member of our organization, you will be responsible for delivering clinical knowledge, experience, and expertise across the entire value chain from ideation to end-of-life.Key...
-
Cambridge, Massachusetts, United States Biogen Full timeJob SummaryWe are seeking a highly skilled Medical Director to lead our US Medical Strategy for Alzheimer's. As a key member of our Specialty Care Medical Director office team, you will be responsible for developing and executing the US medical strategy, tactics, and budget for Alzheimer's in alignment with our global strategy and US budgetary...
-
Cambridge, Massachusetts, United States AAPC Full timeJob Title: Associate Director Medical Affairs Adult Cholestatic DiseasesCompany: Ipsen Biopharmaceuticals IncLocation: Cambridge, MA, United StatesJob Description:Job Summary:The Associate Director Medical Affairs Adult Cholestatic Diseases will support and oversee some of the medical affairs activities of the adult cholestatic therapeutic areas. This role...
Director, Global Medical Affairs
4 months ago
The Role
Moderna is seeking a Director, Global Medical Affairs to spearhead Medical Affairs activities for our Oncology Individualized Neoantigen Therapy (INT) program.
Reporting into the Vice President, Global Medical Affairs Oncology, this role will be the primary point person for the development of INT Medical Affairs plans and strategic activities, including launch plans, data generation, integration, and dissemination.
This role will also define and implement strategy that aligns with business goals by initiating major global projects to close gaps in medical education and research, identifying objectives, innovative tactics and clear measures of success for global activities supporting the launch and lifecycle management of INT.
This is an exciting time to join Moderna as we expand our product reach globally to hundreds of millions of people and experience acceleration in our pipeline and late phase development, thereby poising Moderna for substantial growth in the upcoming years. This role will be a key contributor to Modernas future success in making a transformative impact to patients through our vaccines and therapeutics using our mRNA platform.
Moderna seeks candidates aligned with its culture centered on bold, collaborative, curious, and relentless values, which enable innovation in mRNA-based vaccines and therapeutics to benefit patients.
Heres What Youll Do Provide subject matter area expertise and leadership for cross-functional internal workstreams including Pharmacovigilance, Biostatistics, Clinical Operations, Regulatory Affairs and Brand teams. Develop and foster relationships with external experts, medical societies and patient advocacy groups to ensure that robust insights are consolidated into global plans, enabling the generation of data that are needed by payers, physicians and patients to understand the value of Modernas innovative mRNA platform. Develop innovative research concepts and medical education initiatives to close gaps in research and knowledge and that supports understanding of the benefit/risk profile and optimal use of Modernas INT. Contribute to the writing of manuscripts and abstracts for congress presentations and peer reviewed publications. Create a roadmap for establishing effective internal training on external facing content and data, scientific engagement strategy, processes and systems and lead the preparations of materials for Advisory Board meetings & other key external stakeholder activities. Provide guidance and scientifically accurate review of medical materials and strategies in accordance with established policies and practice standards, including regulatory guidelines to meet various customer needs. Develop and maintain strong, collaborative relationships with the broader Moderna organization. Represent Moderna externally. Heres What Youll Need (Minimum Qualifications) PhD/PharmD required 8+ years of relevant industry experience in Oncology Medical Affairs. Heres What Youll Bring to the Table (Preferred Qualifications) MD, PhD, PharmD Proven ability to act with dynamic range, driving strategy and execution simultaneously to: Develop relevant disease area Medical Affairs strategy and prioritization of activities across multiple workstreams. Deliver high-quality results on time and within expedited timelines. Demonstrated track record in leading cross-functional teams and skillfully removing barriers to encourage collective action towards execution of business goals and priorities. Ability to thrive in a fast-paced, rapidly evolving and dynamic environment, clearly communicating and collaborating with senior leadership to resolve challenging decisions. Keen attention to detail, strong business acumen, excellent analytical, problem-solving, and internal drive to generate high-quality work, with passion and urgency to drive impact for patients. Strong interpersonal and communication skills to meet the needs of varied internal and external stakeholders. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:Highly competitive and inclusive medical, dental and vision coverage optionsFlexible Spending Accounts for medical expenses and dependent care expensesLifestyle Spending Account funds to help you engage in personal enrichment and self-care activitiesFamily care benefits, including subsidized back-up care options and on-demand tutoringFree premium access to fitness, nutrition, and mindfulness classesExclusive preferred pricing on Peloton fitness equipmentAdoption and family-planning benefitsDedicated care coordination support for our LGBTQ+ communityGenerous paid time off, including:
Vacation, sick time and holidays
Volunteer time to participate within your community
Discretionary year-end shutdown
Paid sabbatical after 5 years; every 3 years thereafterGenerous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents 401k match and Financial Planning toolsModerna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit optionsComplimentary concierge service including home services research, travel booking, and entertainment requestsFree parking or subsidized commuter passesLocation-specific perks and extras About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our peopleare the driving force behind our scientific progress and our culture.Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply
Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. Were focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at (EEO/AAP Employer)
-
