- Merck & Co. (North Wales, PA)
- …dataProduce tables and graphics for inclusion in study reports and regulatory submissionsEnsure programmatic traceability from data source to modeling resultSupport ... programming deliverablesproduce SAS transport files and associated documentation for regulatory submissionsRepresent statistical programming on process improvement activitiesEducation and… more
- Merck & Co. (North Wales, PA)
- …and high-quality data to support decision making in clinical trials.-The Associate Principal Scientist , Statistical Programmer supports the ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… 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 ... related drug/vaccine projects in Late Development Statistics.Interacts with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research… 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 ... with Meta Data Repositories.United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the… 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 ... 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
- Organon & Co. (Plymouth Meeting, PA)
- …in Organon Regulatory Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist ( Associate Director) is responsible ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team… more
- Organon & Co. (Plymouth Meeting, PA)
- …the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team… more
- Merck (North Wales, PA)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset ... our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs...GRACS. **Key Functions** + Reports to Executive Director or Associate Vice President, General Medicine + Works Independently and… 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 ... our pipeline and drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs...labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Principal Scientist , Engineering** As part of our Company's Manufacturing Division, the Sterile ... the growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist who is an experienced drug product… more
- Merck (West Point, PA)
- …growing pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist to advance and commercialize the intravitreal ... to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The...As a member of the drug product team, the Associate Principal Scientist will be… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs ... other of our Research & Development Division science. The Associate Principal Scientist is expected...Translational Medicine, Global Medical and Scientific Affairs, and Global Regulatory Affairs and Clinical Safety to identify key issues… more
- Merck (West Point, PA)
- **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments ... group within the Nonclinical Drug Safety organization is seeking an office-based scientist with expertise in impurity risk assessment. A core responsibility will be… more
- Merck (West Point, PA)
- …transfer, and in-line support for large molecule products, including vaccines and biologics. As an Associate Principal Scientist in GVBC, you will play a key ... to develop and optimize real-time process technologies, as well as creating regulatory strategies for the global acceptance of innovative control systems. Your work… more
- Merck (North Wales, PA)
- …analysis and high-quality data to support decision making in clinical trials. The Associate Principal Scientist , Statistical Programmer supports the design, ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Bristol Myers Squibb (Princeton, NJ)
- …difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of the late stage TM ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… 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 ... projects in Late Development Statistics. + Interacts with Clinical, Regulatory , Statistical Programming, Data Management, and other company Research Laboratories… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… 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 ... Data Repositories. + United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
