- 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
- 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
- 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
- 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
- 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
- Olympus Corporation of the Americas (Center Valley, PA)
- …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA) ... @Olympus.com, it is likely not legitimate._ **Job Description** The Complaint Director is responsible for establishing and maintaining a complaint handling process… 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
- 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
- Olympus Corporation of the Americas (Center Valley, PA)
- …work closely with other functions such as Operations, Service, Repair, Post Market Quality, Regulatory Affairs , Medical Affairs and others to ensure that the ... following roles will report into this role directly: Executive Director , Manufacturing Quality (Japan), Director of Quality...Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs … 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 ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … 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 ... **Job Description** Our company is a global health care leader with a diversified portfolio...of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director … more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA) ... role, the Principal Quality Engineer will report to the Director of Post Market Surveillance and will lead the...post market surveillance projects and improvement programs across the global regions (Japan, EMEA, US etc.). This engineer will… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …legitimate._ **Job Description** Working in close alignment with the Executive Director , Compliance Officer/ GRC Business Partner Lead, the Manager, Compliance ... appropriate manner.in an appropriate manner. **Job Duties** + Assists the Executive Director , Compliance Officer / GRC Business Partner Lead with enhancing, further… more