Global Pharmacovigilance & Regulatory Strengthening Lead
$183.41kBioSpace
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 Bachelor’s degree and 7+ years of relevant experience, with travel up to 25% and a hybrid work arrangement. Salary is $183,414 per year, with standard benefits; apply by emailing View email address on click.appcast.io with reference MD0031. #J-18808-Ljbffr BioSpace
$183.41k
...technical oversight on donor-funded projects related to Pharmacovigilance and Regulatory Services Strengthening. Candidates need a Bachelor's degree and seven... ...experience in regulatory affairs. The position supports global health initiatives, requires engagement with...RegulatoryRemote work- 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,... ...single contact for regulatory issues, and leading cross-functional teams. The ideal candidate...RegulatoryWork at office
- 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
$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$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$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- 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
$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$146.3k - $234.1k
...You will be a member of the Global Labeling, Global Regulatory Affairs team and will lead all Labeling activities required for the development and maintenance of the Company Core Data Sheet, US prescribing and patient information and EU CP prescribing and patient information...RegulatoryHourly payWork experience placementLocal areaRemote workWorldwide$216k - $324k
...join Respiratory & Immunology (R&I) as a Global Product Leader (GPL) for an asset in Respiratory... ...perspectives into the process. As the lead ambassador for the product, both... ...balanced focus on safety and efficacy for regulatory approval plus value for market access. Delivering...RegulatoryTemporary workWork at officeFlexible hours3 days per week- 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
$113.85k - $189.75k
Position Summary You will lead Chemistry, Manufacturing, and Controls (CMC) regulatory strategy and execution for mature projects for vaccines. You will manage CMC... ..., ensuring compliance with FDA expectations and global standards. Prepare and review technical regulatory...RegulatoryLocal area- 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 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
- AstraZeneca is seeking a Director of Regulatory Affairs Strategy for cell therapy in the United States. The role focuses on shaping global regulatory strategy for CGT programs spanning... ...and competitive labeling. You will lead cross-functional teams, partner with senior...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
$208.06k - $262.15k
...collaborates with the world’s leading health and science... ..., integrity, and global collaboration. This... ...locations, working to strengthen the supply of safe,... ...scientific integrity, regulatory excellence, and evidence... ...Authorities (NRAs), pharmacovigilance (PV), post‑market...RegulatoryFull timeWork experience placementWork at officeWorldwide- 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
- ...Senior Technical Director, Global Manufacturing Programs, serves... ...across manufacturing, regulatory, market access, and related... ...the organization externally, leading or contributing to engagements... ...and peer institutions, and strengthening strategic relationships that...RegulatoryFull time
- 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
- 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
- ManpowerGroup Global, Inc. is seeking a Lead Business Analyst to work onsite in Rockville, MD, three days per week. The role analyzes automated surveillance systems to detect potential regulatory violations across asset classes, and requires translating regulatory needs...Regulatory3 days per week
- ...Area Units. The Executive Director, Global Product Leader (GPL – Solid Tumor Franchise... .... Typical Accountabilities: · Leads one or more Cell Therapy Global Product Teams... ...all stages of development, coupled with regulatory knowledge · Strong knowledge and...RegulatoryHourly payTemporary work
$249.83k - $374.74k
...As a Global Development Medical Director, you’ll play a pivotal... ...The successful Study Clinical Lead in Late Phase CVRM (... ...Good Clinical Practice, and regulatory requirements. Responsibilities... ...regulatory environment and pharmacovigilance ~ An understanding of pharmaceutical...RegulatoryTemporary workLocal area$154.7k - $290.3k
...Standardization (ISO) guidelines/standards, other global regulatory requirements as outlined in the... ...advanced analytical thought. Lead the governance of core quality systems... ...variety drives excellence and innovation, strengthening our ability to lead in science and...Regulatory- ATCC, a global nonprofit providing biological materials for science and health, is seeking a remote Licensing Manager with deep experience... ...out-licensing agreements for scientific assets. This role leads global licensing strategies, managing international transactions...Remote job
$183.41k
...collaborates with the world’s leading health and science... ...fairness, integrity, and global collaboration. This... ...global locations, working to strengthen the supply of safe, high... ...projects related to Pharmacovigilance (PV) and adjacent Regulatory Services Strengthening (...RegulatoryFull timeWork experience placementRemote workWorldwide- The U.S. Pharmacopeial Convention (USP) seeks a Senior Technical Director for Global Manufacturing Programs to lead technical execution in global health initiatives. This critical role oversees teams, aligns strategies, and represents the organization to external stakeholders...
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