- Gilead Sciences, Inc. (Foster City, CA)
- …concepts, practices, standards, processes and tools + Thorough understanding of global pharmaceutical regulatory requirements and impact on development and ... create possible, together. **Job Description** This position is a member of the Medical Affairs Research (MAR) Leadership Team and will report to the VP, Head of… more
- FleishmanHillard (Washington, DC)
- …provides a fantastic opportunity to work at the intersection of healthcare and public affairs in service to pharmaceutical and medical device companies, as well ... desired areas of expertise include issues advocacy and public affairs campaigns, strong writing skills, and stakeholder engagement with...the best in-class counsel to our roster of remarkable global clients. Are you ready to join the team?… more
- Bausch Health (Bothell, WA)
- Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in ... Cross-functional Collaboration + Act as the key liaison between the global regulatory affairs team and other departments, such as R&D, clinical, quality… more
- Philips (Plymouth, MN)
- **Regulatory Affairs Business Specialist** In this role, you will support regulatory compliance and business objectives for our Image-Guided Therapy Devices business ... education or past experience. + Collaborates with central and regional Regulatory Affairs teams to support establishment registration and listing, and UDI/ Global … more
- Gilead Sciences, Inc. (Foster City, CA)
- …Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic ... and enforcement actions with regards to advertising and promotion of pharmaceutical products. + May initiate and/or contribute to local process improvements… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** The Director of Medical Affairs Research (MAR) is responsible for developing, revising, and implementing the ... research procedural frameworks and cross-functional support for global and local MA research across all therapeutic areas as well as MA-funded externally sponsored… more
- Abbott (Plymouth, MN)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist** to join our team on-site in Plymouth, MN. In this… more
- Organon & Co. (Jersey City, NJ)
- …agile manner. + Provide Regulatory CMC and oversight in developing global Regulatory CMC strategies and executing submissions related to diverse late-stage ... Packages, leading or participating in Agency meetings on CMC topics and executing global initial marketing applications with a line of sight to long-term robust… more
- Abbott (Alameda, CA)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... partnerships .. The individual has department level influence with experience in global regulatory submissions and on-market changes, and is generally recognized as… more
- Bristol Myers Squibb (Princeton, NJ)
- …leads matrixed cross-functional project management teams and projects within the Medical Affairs Cell Therapy Organization. This role reports directly to the Senior ... Therapy Medical organization to deliver key portfolio priorities. Responsibilities include global and regional brand and medical planning, budget planning, congress… more