- Genmab (NJ)
- …a fit? Then we would love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for ... policy and/or intelligence deliverables. This role will be within Global Regulatory Affairs (GRA) and will report...Regulatory Affairs (GRA) and will report to the Sr . Director, Labeling, Policy and Intelligence. The position may… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …including the timely deployment of CDx assays that are compliant with applicable global regulatory guidelines. Collaborates wtih Regulatory Affairs to ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...trials or for approval of CDx. Keeps abreast of regulatory and policy updates in the external environment and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations staff to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …understanding of professional working environment as well as Quality Assurance and global regulatory requirements such that identification of risks is recognized ... oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence...Import/export requirements to the extent that there is overall recognition of global differences exist and understanding… more
- Merck & Co. (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director ( Sr . Principal Scientist) has primary responsibility ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionJoin our Millsboro Senior Leadership team and lead a high-impact Integrated Process Team that directly influences site performance, product quality ... operations, formulation and fill/finish activities.Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and ... the pediatric section of the Vaccine Clinical Development TA.May serve as a senior therapeutic area content expert within the company, providing input into research… more
- Merck & Co. (Upper Gwynedd, PA)
- …create breakthrough science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the ... Job DescriptionOur company is a global health care leader with a diversified portfolio...regulatory reporting, and publication. -- Responsibilities: Specifically, the Senior Director may be responsible for: -Analyzing and summarizing… more
- Merck & Co. (Boston, MA)
- …experience in drafting regulatory documents and interactions with global regulatory agencies requiredSelf-driven leader willing to advance Precision ... Job Description Senior Principal Scientist, Precision Medicine, Immunology Precision Medicine...created Precision Medicine and Diagnostics function. Reporting to the Associate Vice President ,Precision Medicine and Diagnostics, in this… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Associate Director, Medical Education - Oncology, is responsible for the strategic planning and ... MA training modules). The focus of these plans and activities will be either global , US-focused with intended use and adaptation by other regions globally, or solely… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … Knowledge: Deep understanding of FDA, EMA, and other global regulatory requirements for pharmaceutical manufacturing.Operational Excellence: Expertise ... Legend Biotech is a global biotechnology company dedicated to treating, and one...daily production schedules.Will have 3-6 direct reports ranging from Associate Director, Senior Manager, and Manager.Oversee the… more
- BC Platforms (Somerville, MA)
- …data insights. We have the unique ability to provide unmatched access to global , research-ready, regulatory -grade patient data. This is enabled by an end-to-end ... change in the life sciences industry. If you're ready to work with global clients, cutting-edge solutions, and a mission-driven team, we'd love to hear from… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director, Global Regulatory Lead (GRL), reporting to the Executive Director, Senior Director or ... Associate Director will be responsible to: + Develop regulatory strategy for their assigned products, in order to...regulatory expert on those projects. + Lead the Global Regulatory Teams, which coordinates cross-functional … more
- CSL Behring (King Of Prussia, PA)
- …to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director Global Regulatory Lead, EHT ? The job is in ... and related delivery teams. Lead discussion at Global Regulatory Forum (GRF) or with senior management on projects. *Lead GRA project deliverables (eg, Core… more
- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA ... medicine promotion. **How you will contribute:** + As our Associate Director, Global Regulatory Affairs...if there is new data or campaigns that require senior level management input or alignment. + Strategic business… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ... you thought was possible. Ready to get started? **Main Responsibilities:** + Represents Global Regulatory Affairs (US RA AdPromo) as a member of… more
- Teva Pharmaceuticals (West Chester, PA)
- …matter expert and will manage the processes and procedures to ensure compliance with global regulatory requirements. The Associate Director will partner with ... Associate Director, Transparency and Disclosure Date: Sep 8,...and Disclosure (T&D) is responsible for leading and managing global Transparency & Disclosure activities. This role will serve… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position ... Summary:** The selected candidate will have leadership responsibility for global regulatory strategy within a development team...issues, and risks in written and verbal format to regulatory senior leadership team and other governing… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …and regions. **Hours:** Day Shift - Monday through Friday: 8:00 am to 5:00 pm ** Sr . Quality Associate I / II / Principal, Quality Assurance:** The Senior ... and manufacturing process from pooling to packaged final container is preferred. The Senior Quality Associate II- Additional responsibilities in addition to the … more
- Santander US (Miami, FL)
- Sr . Technology Risk Associate Country: United States of America **Your Journey Starts Here:** Santander is a global leader and innovator in the financial ... **We Want to Talk to You!** **Position Summary:** The Sr . Technology Risk Associate is responsible for...of Technology risks. An excellent understanding of the evolving regulatory landscape in the US and EU are vital… more
