- West Pharmaceutical Services (Exton, PA)
- …+ Works with global Regulatory Affairs colleagues, Quality Assurance and Research & Development teams to ensure submissions are accurately prepared and ... comply with global regulations + Provide leadership to product development teams for regulatory issues and questions...Bachelor's with 5+ years of medical device, pharmaceutical or regulatory experience + Master's degree/ PhD with 3+… more
- Sumitomo Pharma (Harrisburg, PA)
- …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... HTA submissions. The individual will be responsible for leading development of all non-clinical and clinical regulatory ...the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and… more
- West Pharmaceutical Services (Exton, PA)
- …**Work Experience** + Bachelor's with 5+ years required; or + Master's degree/ PhD 2+ years medical device regulatory experience required **Preferred Knowledge, ... involves sitting most of the time. **Additional Requirements** + Ability to research , read, analyze, and interpret regulatory literature and documentation,… more
- J&J Family of Companies (Spring House, PA)
- …Support, Mentorship, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development , Regulatory ... The Director, Global Regulatory Leader in Global Regulatory Affairs will be responsible for the development...requirements and guidelines specific to the areas of clinical research , product development , and labeling is required.… more
- West Pharmaceutical Services (Exton, PA)
- …quality documentation with a high degree of confidentiality. + Ability to research , read, analyze, and interpret regulatory literature and documentation, ... Senior Regulatory Affairs Specialist Requisition ID: 71673 Date: Nov...of professionals with opportunities for lifelong learning, growth and development . Supported by benefit programs, we empower the physical,… more
- Merck (North Wales, PA)
- …Curiosity, Interdisciplinary Problem Solving, Neuropathic Pain, Neuroscience, Neuroscience Research , Pain Management, Pharmaceutical Development , Regulatory ... development , including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
- Merck (Upper Gwynedd, PA)
- …Awareness, Cross-Functional Teamwork, Drug Development , Ethical Standards, Medical Research , Oncology, Pulmonology, Regulatory Requirements, Research ... development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
- Merck (Upper Gwynedd, PA)
- …study reports, or publication; and + Participation in internal and joint internal/external research project teams relevant to the development of new compounds ... regulatory affairs, statistics, and manufacturing to manage clinical development projects + Assist the Senior Director, Associate Vice-President/Vice-President… more
- Merck (North Wales, PA)
- …Clinical Trial Support, Cross-Functional Teamwork, Drug Development , Medical Research , Pharmaceutical Development , Pulmonology, Regulatory Reporting, ... study reports, or publication + Participating in internal and joint internal/external research project teams relevant to the development of new compounds,… more
- Carnegie Mellon University (Pittsburgh, PA)
- …to technical execution, this role demands leadership in mentoring and team development . The Research Scientist will supervise and support graduate students, ... Carnegie Mellon University is a private, global research university that stands among the world's most...and deeply translational. The successful candidate will guide the development of novel software tools for organ blueprint generation… more