- Merck (Upper Gwynedd, PA)
- …reliable, and compliant medical products, practices and solutions to the world. The Associate Principal Scientist Regulatory Affairs supports products ... research on regulatory guidances or competitive intelligence. The Associate Principal Scientist will have responsibility for driving results for… more
- Merck (West Point, PA)
- …the growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist who is an experienced drug product ... transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group… more
- Merck (Upper Gwynedd, PA)
- **Job Description** **Title: Associate Principal Scientist / Associate Director, Outcomes Research** **Role Summary** + Under the guidance of a senior ... leader, an Associate Principal Scientist / Associate ...reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs… more
- Merck (West Point, PA)
- …in the pre-clinical space as screening reagents or vaccines. The candidate for this Associate Principal Scientist position is expected have strong technical ... developing junior scientists, while pursuing partnerships with academic, industry, and regulatory bodies to enhance research efforts and scientific reputation. +… more
- Merck (Lower Gwynedd, PA)
- …and expanding your career. We are seeking a highly motivated Senior Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalysis ... as well as selecting and designing applicable assays capable to meet regulatory expectations for vaccine or biologics development. The candidate should be current… more
- Merck (West Point, PA)
- …process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative direction of ... functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and… more
- Merck (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Merck (North Wales, PA)
- …to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs. + In ... collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications. + Responsible for… more