- 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
- Chemours (Wilmington, DE)
- …improvement at a time. Chemours is seeking a ** Director of Regulatory Advocacy** to join our growing **Government Affairs ** team! This position ... **Washington, DC** office. The successful candidate will join Chemours' Global Government Affairs Group with a primary...Group with a primary responsibility for supporting US federal regulatory affairs engagement with the United States… 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
- Merck (North Wales, PA)
- …including the related SOPs and Execution resources. The incumbent is accountable to Sr. Director of Business Process and Systems with input from VP, CSRM as needed, ... contributing functional areas and process governance committees. Works with Sr. Director for Business Process and Systems, CSRM to develop and implement… 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
- 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 (Philadelphia, 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 (Philadelphia, 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 (Philadelphia, 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
- Publicis Groupe (Philadelphia, PA)
- …Health** Digitas Health is the _Agency of Now_ : the first global connected-health agency, purpose-built for marketing today. Digitas Health specializes in helping ... | Twitter: www.twitter.com/digitas_health **Job Description** **Position Summary** The Medical Director oversees the accuracy and relevance of scientific content… 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