- Merck & Co. (North Wales, PA)
- Job DescriptionDescription: The Associate Principal Scientist , Oncology Publications Medical Writing, works with scientists in our company's Research Labs ... program, as well as select early-stage development projects and our company's science. The Associate Principal Scientist is expected to collaborate with our… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... support for translational oncology projects and studies.-Interact with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research… more
- Merck & Co. (North Wales, PA)
- …and dedicated colleagues while developing and expanding your career.The Clinical Director ( Principal Scientist ) has primary responsibility for the planning and ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be responsible… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Principal Scientist is responsible for developing and implementing Regulatory CMC strategies for ... with global regulations and guidance's, and Company procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Merck (North Wales, PA)
- **Job Description** **Description:** The Associate Principal Scientist , Oncology Publications Medical Writing, works with scientists in our company's ... program, as well as select early-stage development projects and our company's science. The Associate Principal Scientist is expected to collaborate with our… more
- Merck (North Wales, PA)
- **Job Description** The Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug/vaccine ... 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)
- …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)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... translational oncology projects and studies. + Interact with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research Laboratories… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more
- Merck (North Wales, PA)
- …dedicated colleagues while developing and expanding your career. The Clinical Director ( Principal Scientist ) has primary responsibility for the planning and ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may be… more
