- J&J Family of Companies (Spring House, PA)
- Associate Director, CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director, CMC Regulatory ... the product and is in alignment with the strategies of global regulatory affairs , the therapeutic area, commercial, regional functions and the Quality Target… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate ... will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and… more
- Merck (North Wales, PA)
- …Director/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Merck (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help ... drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs Liaison is responsible for development...labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice… more
- Merck (North Wales, PA)
- …Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation… more
- Veterans Affairs, Veterans Health Administration (Philadelphia, PA)
- …as collecting data and tracking risk management indicators. Represents the Chief and Associate Chiefs, Pharmacy Service, in their absence or conflict in schedule, in ... assure that administrative activities follow appropriate standards and applicable regulatory entities. Financial and Resource Management: Typical duties include… more
- Takeda Pharmaceuticals (Exton, PA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... of my knowledge. **Job Description** Join Takeda as an Associate Director, US Advertising & Promotion Regulatory ... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- University of Pennsylvania (Philadelphia, PA)
- …resources, and much more. Posted Job Title Quality Assurance Specialist ( Regulatory ) CVPF(Center for Cellular Immunotherapy) Job Profile Title Research Coordinator ... to help with raw materials release, new hire QA Associate train. Position contingent upon funding. Qualifications + Bachelor...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
- Pfizer (Collegeville, PA)
- …digital communication boards, visuals / posters / signage, etc.). The Sr Associate will serve on cross-site projects and provide communications support related to ... operations, data management, and procurement activities. As a Sr Associate , your knowledge and skills will contribute towards the...the goals and objectives of the Pfizer Collegeville Site Affairs team. Your focus and ability to meet team… more
- Organon & Co. (Plymouth Meeting, PA)
- …and development operations across the functions (Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs ) and the drug ... of industry experience in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.) + At least… more
- Merck (North Wales, PA)
- **Job Description** **Job Description:** The Associate Director, Marketing, HPV Scientific Strategy plays a critical role in supporting the HPV vaccine franchise. ... resources to address the opportunities. + Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center… more
- J&J Family of Companies (Horsham, PA)
- Associate Director, Real World Value and Evidence Oncology Solid Tumor - 2406221056W **Description** Johnson & Johnson is currently recruiting an Associate ... humanity. Learn more at https://www.jnj.com/. In this in-house position, the Associate Director, RWV&E, will be responsible for conducting real-world evidence… more
- Merck (North Wales, PA)
- …under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) organizations ... Provide financial planning, forecasting and analytical support to ourResearch&DevelopmentDivision, Global Regulatory Affairs & Clinical Safety (GRACS), and QA… more
- Merck (Upper Gwynedd, PA)
- …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... **Job Description** The Associate Principal Scientist, General Medicine Publications Medical Writing,...other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title VPSE C2L PHL Associate Director Job Profile Title Associate Director B, Student Services, Student ... Job Description Summary Reporting to the Director of VPSE C2L-PHL, the Associate Director is responsible for leading, developing, articulating, and implementing best… more
- Fujifilm (Warminster, PA)
- …+ Collaborate effectively with cross-functional teams, including researchers, quality control, and regulatory affairs , to meet project goals and timelines. + ... America Corporation reporting to FUJIFILM Holdings Corporation. We are hiring an Associate Scientist. The Associate Scientist will conduct protein purification… more
- Merck (West Point, PA)
- …drug metabolism, process chemistry, analytical chemistry, manufacturing, and regulatory affairs . Other responsibilities include conducting literature/database ... **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments to… more
- WuXi AppTec (Philadelphia, PA)
- …in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC dossiers to ... support global filings for TIDES new drug applications. **Job Summary:** Responsible for managing projects within WuXi-TIDES, WuXi's API development and manufacturing division for Oligonucleotides and Peptides. Leads the orderly progression of projects from… more
- Organon & Co. (Plymouth Meeting, PA)
- …in supporting ongoing clinical research and interface extensively with Clinical Development, Regulatory teams, and Medical Affairs , among other internal teams, ... **Job Description** **The Position** Reporting to Associate Vice President of Clinical Data Sciences (AVP...statistical input and expertise in the clinical development and regulatory submission and be responsible for statistical strategies and… more
- University of Pennsylvania (Philadelphia, PA)
- …Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work closely ... of the team's work, working closely with the CRU Regulatory coordinators to manage, review and initiate trials to...+ The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's,… more