Global Regulatory Lead for Vaccines & Infectious Diseases
Merck
Merck is looking for a Principal Scientist in Regulatory Affairs at its Rockville, Maryland office. The role involves developing global regulatory strategies for vaccine projects, acting as the single contact for regulatory issues, and leading cross-functional teams. The ideal candidate will possess an M.D. or Ph.D. with extensive experience in drug development and regulatory affairs. This position requires strong analytical skills, excellent communication, and leadership in collaborative settings. At Merck, we offer a comprehensive benefits package and a hybrid work environment. #J-18808-Ljbffr Merck
- Merck & Co. is hiring a Principal Scientist for Regulatory Affairs in Rockville, MD. This role focuses on developing global regulatory strategy for vaccine and infectious disease projects. The successful candidate will lead the Global Regulatory Team, coordinate cross-...Regulatory
$210.4k - $331.1k
Job Description Regulatory Affairs Headquarters Principal Scientist... ...and implementation of global regulatory strategy for their... ...assigned projects in the Vaccines and Infectious Disease therapeutic area.... ...the product life cycle. Lead the Global Regulatory Team...RegulatoryFor contractorsWorldwide$210.4k - $331.1k
Overview The Regulatory Affairs Headquarters Principal Scientist... ...and implementation of global regulatory strategy for their... ...assigned projects in the Vaccines and Infectious Disease therapeutic area. Department... ...of drug development. Leads cross-functional efforts to...RegulatoryFor contractorsLocal areaWorldwideRelocationVisa sponsorshipFlexible hoursShift work- ...towards the improvement of global public health– join... ...further elevate the Infectious Disease unit in one of the... ...indications in the field of vaccines Help invent,... ...Safety, Biometrics, Regulatory Affairs, Clinical Operations... ...Building on this, we lead the way into the...RegulatoryHourly payTemporary workWork at office3 days per week
$183.41k
...oversight on donor-funded projects related to Pharmacovigilance and Regulatory Services Strengthening. Candidates need a Bachelor's degree and... ...of experience in regulatory affairs. The position supports global health initiatives, requires engagement with stakeholders, and...RegulatoryRemote work- Women In Bio is seeking a professional to lead CMC regulatory strategy for vaccines in Rockville, Maryland. This role requires deep knowledge of FDA regulations, development processes, and collaborative skills with cross-functional teams. The ideal candidate has at least...Regulatory
- The National Institute of Allergy and Infectious Diseases (NIAID) within the National Institutes of Health seeks a Scientific Program Manager to support vaccine development programs, provide therapeutic and programmatic analysis, and advise investigators. This role involves...
- JobRx, Inc. is seeking a Regulatory Affairs Manager (RAM) based in Gaithersburg, Maryland, to lead the end-to-end planning and execution of regulatory deliverables. The RAM plays a key role in regulatory submissions, providing strategic insights and managing regulatory...Regulatory
$200k - $220k
Precigen is seeking an Associate Director/Senior Manager, Regulatory Affairs in Germantown, MD. The role involves managing regulatory affairs... ...and commercial products and ensuring compliance with global regulatory requirements. The ideal candidate should possess a bachelor...RegulatoryFull time$276.13k - $414.19k
AstraZeneca is seeking an Executive Director for Regulatory Affairs Strategy, specializing in Cell & Gene Therapy, based in Gaithersburg, MD. This role involves setting global regulatory strategy for advanced therapies, ensuring timely approvals, and engaging with health...Regulatory$154.7k - $290.3k
...implementing the Quality Management System to ensure compliance with regulatory standards in the pharmaceutical industry. The role involves... ...team while driving continuous improvement across various global locations. The ideal candidate will possess over 10 years of experience...Regulatory- ...Scientific Program Manager at the National Institutes of Health (NIH) in Bethesda, MD. The role involves overseeing regulatory affairs related to vaccines and ensuring compliance with FDA regulations. Ideal candidates will possess a Master’s degree and 8-10 years of...Regulatory
$113.85k - $189.75k
Position Summary You will lead Chemistry, Manufacturing, and Controls (CMC) regulatory strategy and execution... ...mature projects for vaccines. You will manage CMC regulatory... ...talent to get ahead of disease together.... ...with FDA expectations and global standards. Prepare and...RegulatoryLocal area- GlaxoSmithKline is looking for a highly experienced regulatory professional to lead Chemistry, Manufacturing and Controls (CMC) strategy. This role involves collaboration across development, manufacturing, and regulatory teams to ensure compliance and timely access to medicines...Regulatory
$183.41k
U.S. Pharmacopeial Convention (USP) in Rockville, MD seeks to provide technical oversight on donor-funded PV and RSS projects, collaborating with NRAs and regional bodies to strengthen the pharmacovigilance framework and international guidelines. The position requires a...Regulatory$100k - $200k
We are seeking a proactive and execution‑oriented Global Benefits Lead to help scale and optimize our global benefits programs. Reporting to... ..., COBRA, HIPAA, nondiscrimination testing, and other U.S. regulatory requirements. Partner with regional stakeholders to support...RegulatoryLocal area$216k - $324k
...Respiratory & Immunology (R&I) as a Global Product Leader (GPL) for an... ...into the process. As the lead ambassador for the product,... ...be responsible for: Ensuring disease strategy is innovative, with... ...focus on safety and efficacy for regulatory approval plus value for...RegulatoryTemporary workWork at officeFlexible hours3 days per week- ...Senior Medical Director, Global Clinical Development (Infectious Disease/Pulmonology) Hybrid role: 3 days per week... ...at internal governance meetings Lead the Clinical Team and work closely... ...Patient Safety, Biometrics, Regulatory Affairs, and Clinical Operations...RegulatoryHourly payTemporary workWork at officeFlexible hours3 days per week
- ...The Director of Bacterial Vaccine Discovery in Early Infectious Disease leads efforts to discover and develop bacterial... ..., Bioprocess Development, and Regulatory Affairs, as well as managing external... ...and Translational Medicine, and Global Project Teams to ensure cross-...RegulatoryHourly payContract workTemporary work
- Hilton is seeking a Senior Counsel & Global Franchise Regulatory Leader based in our corporate office in McLean, VA. You will oversee Hilton's global... ..., and cross-jurisdiction compliance to support expansion. Lead a team of attorneys and paralegals, collaborating with...RegulatoryWork at office
$331.87k
...Job Description: Global Clinical Head- Executive Director... ...further elevate the Infectious Disease Therapy Area in one of... ...Plan (CDP), and regulatory documents (e.g., briefing... ...ability to lead the development of a program... ...Infectious disease and/or vaccine expertise • Named Investigator...RegulatoryHourly payTemporary workWork at officeFlexible hours3 days per week- The Fountain Group seeks a Regulatory Affairs Director in Gaithersburg, MD to provide strategic and operational regulatory leadership... ..., and lifecycle management of assigned products. As global/regional lead, you will influence health authorities, craft clinical strategies...Regulatory
- AstraZeneca is seeking a Director of Regulatory Affairs Strategy for cell... ...The role focuses on shaping global regulatory strategy for CGT... ...oncology and immune-mediated diseases, translating breakthrough... ...competitive labeling. You will lead cross-functional teams, partner...Regulatory
- AstraZeneca in Gaithersburg, MD, seeks a Director of Regulatory Affairs Strategy for Cell Therapy. You will shape global regulatory pathways for advanced therapies,... ...with patient needs and business goals. You will lead regulatory design, filings, and interactions with...Regulatory
- ...years of experience in planning and a strong understanding of regulatory compliance in the pharmaceutical industry. Key responsibilities... ...include managing the materials planning process, collaborating with global teams, and developing process improvements. An inclusive...Regulatory
- ...travel, totaling between 50-60% of the year. The ideal candidate will manage program delivery resources, lead client engagements, and ensure adherence to regulatory standards. Candidates should have over 10 years of experience in intelligence or special forces and the ability...RegulatoryRemote jobOverseas
- ...biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare... ...ICH GCP, and all applicable regulatory requirements. The CRA will conduct... ...health initiatives, both globally and in our local communities...RegulatoryWork experience placementInterim roleCasual workLocal areaRemote workWork from homeFlexible hours
- AstraZeneca seeks a Senior Director of Regulatory Affairs Strategy for Cell Therapy to spearhead global regulatory vision across multiple indications. You will guide... ...commercial teams to accelerate patient access. You will lead a global regulatory strategy team, collaborate...Regulatory
- USP, based in Rockville, MD, seeks a Senior Director, Global Programs (Regulatory and Laboratory) to lead a global growth strategy for externally funded regulatory and laboratory programs. The role oversees a distributed team, develops partnerships with funders, and represents...Regulatory
- The Regulatory Affairs Manager (RAM) is a regulatory specialist with project management capabilities responsible for leading the end‑to‑end planning, coordination, and execution of assigned deliverables... ...requirements to GRET (Global Regulatory Execution Team), GRST (Global...Regulatory
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