. Could you be our next Associate Director, Global Regulatory Affairs? The job is located in our King of Prussia PA office. This is a hybrid position.... You will report to the Director of Global Regulatory Affairs. Responsibilities: You are a member of a Regional Therapeutic Area...
. We are looking for a driven and motivated Global Regulatory Affairs Director who will be instrumental in developing and executing global... in regulatory affairs. Awareness of global regulatory processes, including submission and approval activities. Understanding...
an Associate Director to lead the Molecular lab within the Late Development (AdVAnce) Vaccines bioanalytical group located... power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through...
of Global Regulatory Affairs, you will be responsible for leading regulatory strategy for mRNA Vaccines assets, securing product... products. The Associate Director will be accountable to the Asset GRL (Global Regulatory Lead) for development of appropriate...
The Director Scientific Lead, Interventional Studies will lead and oversee the execution of the Vaccines/Oncology... sponsored clinical trials by the medical affairs organization (non-regulatory label directed programs). This pivotal role...
Job Title: US Medical Director- Portfolio, New Products, Innovation- Vaccines Location: Bridgewater, NJ About the... and backgrounds which strengthens our team and mirrors the healthcare communities we engage. We are an innovative global healthcare...
Job Title: US Medical Director, Mainline Vaccines Location: Bridgewater, NJ / Morristown, NJ About the Job The... Responsibilities: The US Medical Director, Mainline Vaccines, will contribute to development and execution of the medical...
Position reports to: Head, Federal Government Affairs Location: Person must be commutable to our Washington, DC... with their Congressional colleagues. Identify Opportunities and Risks: Continuously monitor legislative and regulatory landscapes...
Regulatory TA Head. You will play an important leadership role as part of the Global Regulatory Affairs (GRA) GPS Leadership...), Clinical Development Team (CDT), and within Global Regulatory Affairs (GRA). Experience Bachelor's degree (four-year...
) reviewers. The Director will provide consultative support to Global Regulatory Affairs therapeutic project teams for issues...As the Director, Regulatory Advertising & Promotion Policy, you will be responsible for leading assigned products...
) reviewers. The Director will provide consultative support to Global Regulatory Affairs therapeutic project teams for issues... portfolio. As the Director, Regulatory Advertising & Promotion Policy, you will be responsible for leading assigned products...
lifecycle of the asset. Will create and manage integrated regulatory plans, for purposes of operationalizing the Global... and maintain a holistic view of the global regulatory integrated plan at the asset level for operationalizing the Global Regulatory...
The Opportunity The Senior Director, Global External Partnerships Strategy is an important role reporting into the VP..., you will work with our teams across Enterprise Global Business Development, Global Commercial Development, R&D, Medical Affairs...
applications. Other functional groups represented on the team include project management, regulatory affairs, global clinical... global environment in which the company operates. The Medical Director/Senior Medical Director assists in the preparation...
studies as well as the preparation of the summary documents needed for a global submission to regulatory authorities... with Regulatory Affairs in the preparation of regulatory interactions. Contribute significantly to the preparation, drafting...
teams, including Clinical Development, Regulatory Affairs, Biostatistics, Clinical Data Management, Clinical Supplies...Job Title: Associate Director, Clinical Operations Job Location: San Carlos, CA, USA Job Location Type: Remote...
, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may.... Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics...
by the medical affairs organization (non-regulatory label directed programs). This pivotal role requires a leader with deep... expertise in industry sponsored clinical research & global medical affairs, have significant commercial acumen, and cross...
, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may.... Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics...
, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may.... Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics...