- Teva Pharmaceuticals (West Chester, PA)
- Senior Director Regulatory Affairs CMC (Biologic Products) Date: Jun 13, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... to make a difference with. **The opportunity** The Sr. Director , Global Regulatory Affairs CMC...strategy and assessing the quality of documents for regulatory submissions to major market health authorities as well… more
- J&J Family of Companies (Spring House, PA)
- …Medical Affairs programs/activities globally. **Key Responsibilities:** Develop Global Medical Affairs strategy and plan for the assigned compounds based on ... Global Medical Affairs Leader, Director , Dermatology - 2406179906W...Excellent knowledge of study execution, benefit risk management and regulatory affairs . + Proven ability to act… more
- J&J Family of Companies (Horsham, PA)
- Associate Medical Director , Rheumatology Therapeutic Area - Medical Affairs - 2406188235W **Description** Johnson & Johnson is recruiting for an Associate ... humanity. Learn more at https://www.jnj.com/. As a member of Immunology (IMM) Medical Affairs , the Associate Medical Director , Rheumatology TA will assist in… more
- J&J Family of Companies (Horsham, PA)
- …an Associate Director , Clinical Scientist to join our world-class Medical Affairs Gastroenterology Therapeutic Area Strategy Team located in Horsham, PA. Are ... Associate Director , Clinical Scientist- Gastroenterology Therapeutic Area - Medical Affairs - 2406185119W **Description** Johnson & Johnson is currently seeking… more
- American Water (Norristown, PA)
- …senior-level communications counsel and ensures the effective implementation of external affairs and related communications activities. Assists in strategy ... state including Customer Communications Manager, the Internal Communications Manager, the Director of Communications and External Affairs , the Customer Service… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …Director , GRO Regulatory Project Management and be a part of the Global Regulatory Affairs Team. **How you will contribute:** + As Associate Director , ... goals and regulatory submissions in accordance with regulatory strategy for moderately complex programs and...through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global … more
- Pfizer (Collegeville, PA)
- …willing to learn and advance in their career. As well as supporting the regulatory strategy from a regional perspective, you will partner with project teams ... regulatory science * Provide regional strategic regulatory expertise as regulatory representative to Global Regulatory Strategy Team (GRST). * Lead… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... and implementation of labeling content and strategy of assigned product(s) in various stages of drug...with Health Authorities. + Ensures labeling content conform to regulatory requirements. Management of Local Exceptions and LOC Interactions… more
- Pfizer (Collegeville, PA)
- …digital and social media solutions that align to the impact the Global Medical Affairs strategy and shape the digital roadmap and quickly deliver highest value ... affairs , commercial, corporate communications, medical content, Integrated Media Strategy , digital/OSS, and other key stakeholders to ensure alignment across… more
- J&J Family of Companies (Horsham, PA)
- …continuous improvement and developing trusting partnerships internally (eg R&D, Quality, Regulatory , Commercial, Legal, Medical Affairs ) and externally (eg ... Sr. Director , Senior Safety Officer- Johnson & Johnson Enterprise...is preferred. Additional education or experience in clinical, medical affairs , regulatory , epidemiology or biostatistics preferred +… more
- Teva Pharmaceuticals (West Chester, PA)
- …as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing, ... key documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director will provide input to the… more
- J&J Family of Companies (Spring House, PA)
- …quality monitoring & compliance, data management, global medical safety, biostatistics, regulatory affairs , clinical supplies unit, medical writing, clinical ... pharmacology, legal, finance, quality assurance, strategy and operations, global medical affairs , health...Committee (IDMC) and adjudication meetings as needed. + Assists Regulatory Affairs in determining requirements for any… more
- J&J Family of Companies (Horsham, PA)
- …Sales, Sales Training, Commercial Excellence, Finance, Strategic Customer Group, Medical Affairs , HECOR, Global Commercial Strategy , R&D, New Business ... Director of Marketing (DOM), Prostate Portfolio - 2406189783W...be responsible for the development of an integrated US strategy , directing all marketing activities and the design, planning,… more
- J&J Family of Companies (Horsham, PA)
- Director , Medical Safety Officer, Oncology - 2406183977W **Description** Johnson & Johnson, is recruiting for a Director , Medical Safety Officer, Oncology to be ... benefit/risk. The MSO will report to the GMS Sr. Director Product Safety Head, Oncology and oversee the safety...Area Safety Head (TASH), the Head of Global Safety Strategy & Risk Management (GSSRM), the Chief Safety Officer… more
- J&J Family of Companies (Trenton, NJ)
- …partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs , clinical pharmacology, health economics, and the disease ... Medical Director / Sr. Med Director , Clinical Research...the clinical leader for product evaluation and develops the strategy and the content for regulatory documents.… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met ... therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible...+ Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... and implementation of labeling content and strategy of multiple assigned products in various stages of...assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions… 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
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Research Director D (Department of Neuropsychiatry) Job Profile Title Director D, Research ... to the study of brain and behavior throughout the lifespan. The Research Director D will support the Section Director , Program Directors and Investigators… more
- Organon & Co. (Plymouth Meeting, PA)
- …stakeholders, including Medical Affairs , Sales, Marketing, HCP Engagement, Compliance and Regulatory . The role will report to the Director , US Medical ... collaboration skills, including cross-divisionally with colleagues from Sales, Medical Affairs /Clinical, Compliance/Quality, and Regulatory . + Experience working… more