- Merck (North Wales, PA)
- **Job Description** Our Diagnostics focused Regulatory Affairs team helps bring new precision medicine advancements to the world by facilitating effective, ... as appropriate, and corresponding therapeutic dossiers. + Interacting with global regulatory authorities and diagnostic partners to...devices, the majority of which must be in diagnostic regulatory affairs . Preferred: MS with minimum of… more
- Merck (North Wales, PA)
- …The GRACS Global Process Lead (GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business ... compliant business standards, process maps, and risk management for global processes across GRACS. The GPL actively engages with...+ Complete Impact assessment on new or changed external regulatory policies as it pertains to the processes that… more
- Merck (North Wales, PA)
- …standards and policies and business objectives. Actively participate in labeling and global regulatory team meetings to ensure support for anticipated ... **Job Description** Reports to the Director /Senior Director in the Office of...all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to… more
- Takeda Pharmaceuticals (Exton, PA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... and compliance with regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the organization. Identify … more
- Merck (North Wales, PA)
- …Scientific Leaders; and ensure all Scientific Leader engagement activities comply with regulatory , legal, and ethical standards + Commercial lead in driving engaging ... Vaccines Franchise brands at Congresses; identifying strategic congresses for Global support, including key regional congresses, aligning team activities, and… more
- Pfizer (Collegeville, PA)
- …lead or participate in manuscript, abstract and poster development. + Safety and Regulatory Support: Provide regional medical affairs support and leadership for ... in Breat Cancer Franchise on behalf of Asset Medical Affairs team. + Provides strategic medical input for breast...at each lifecycle stage. + Partnership cross-function partners within Global team + Promotional Materials Development and Review: +… more
- Takeda Pharmaceuticals (Exton, PA)
- …potential issues. POSITION ACCOUNTABILITIES: + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations ... the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Merck (North Wales, PA)
- …above-product public policy issues and geo-political changes that will impact our global business. The Director independently and proactively identifies risks ... Director , Policy Development, Strategy, and Capabilities, the AVP, and VP Global Public Policy. Reporting to the Executive Director , Policy Development &… more
- Merck (North Wales, PA)
- …and must be able to work with all levels of management within and outside of Global Regulatory Affairs and Clinical Safety (GRACS). + Interact closely with ... **Job Description** Under minimal guidance of the Executive Director / Director /Associate Director , Pharmacovigilance (PV)... regulations. + The incumbent must be knowledgeable of global regulatory requirements at a general level… more
- Merck (North Wales, PA)
- …Associate Director will independently develop and execute a company-wide global policy advocacy strategy, create business cases for and manage budgetary ... **Job Description** **Position Description:** **Associate Director , Policy Advocacy** The Associate Director ,...Policy Advocacy serves as the senior expert in the Global Public Policy (GPP) organization on designing and implementing… more
- CSL Behring (King Of Prussia, PA)
- …also partner with teams from Global Commercial Development, Clinical Research and Regulatory Affairs to ensure North America is represented on all future ... **CSL Behring is seeking a Sr. Director , New Product Planning & Evidence Generation (US...multiple teams and people including marketing leadership, US Medical affairs , US Health Care Systems teams, global … more
- Teva Pharmaceuticals (West Chester, PA)
- Director , Clinical Statistics Date: Sep 19, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 57783 **Who we ... and new people to make a difference with. **The opportunity** The Director , Clinical Statistics is a skilled statistician with significant experience in drug… more
- Merck (North Wales, PA)
- …the Policy Development Director in conducting analyses to produce reports on global policy environment as requested by Executive Director , AVP, other GPP LT ... **Job Description** **Position Description:** **Associate Director , Policy Strategy and Capabilities** The Associate ...to ensure that they are fit for purpose for global , regional, and country policy planning and activity tracking.… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
- CSL Behring (King Of Prussia, PA)
- …refining and improving standards for these deliverables. + Collaborate with R&D, Regulatory Affairs , Medical Affairs , Marketing, and other partner ... **Role Overview:** The Executive Director of Global Market Access for Pipeline Assets will be responsible for shaping and implementing market access strategies… more
- Merck (Upper Gwynedd, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director of Field Reimbursement is a key role at CSL and member of the US patient experience leadership team. The role is one of two Field ... patient experience, marketing, sales, health care systems, policy advocacy and government affairs (PAGA), medical affairs . + Oversee and champion reimbursement… more
- Pfizer (Collegeville, PA)
- …and corporate campaigns and brand acts that build trust and brand equity. The Director , Brand Campaigns is a critical member of this team responsible for leading the ... and ambitious marketer to develop breakthrough campaigns that inspire and engage global audiences and drive affinity and awareness for a world class healthcare… more
- Organon & Co. (Plymouth Meeting, PA)
- …innovation and promotional regulatory strategy in collaboration with Commercial, PRT, Global Regulatory Liaisons, Medical Affairs and Worldwide Product ... + Support BD due diligence efforts and define promotional regulatory risks of asset acquisitions and partnerships. + Leads...live their best lives. We are a $6.5 billion global healthcare company focused on making a world of… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more