- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Principal Scientist , Sterile Drug Product Commercialization** As part of Our Company's ... biologics, and pharmaceutical products and combination products. We are seeking an experienced Associate Principal Scientist to advance and commercialize a… 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)
- …create a healthier future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with experience in Vaccine biology or ... professional development. + Properly document protocols and findings, author preclinical regulatory documents, and comply with all laboratory safety requirements. +… 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)
- …in compliance with departmental and company Standard Operating Procedures, regulatory requirements, and standards. **Primary Activities** **:** + Business System ... processes, assuring they are of high quality and complaint with regulatory requirements **Skills** **Education and Minimum Requirement** **:** + BA/BS in… 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 (West Point, PA)
- **Job Description** Our Company a global healthcare leader, is seeking an Associate Principal Scientist to join our collaborative, dynamic, and inclusive ... diverse, dynamic, AAALACi-accredited animal research institution. Collaborate cross-functionally with principal investigators, scientific staff, toxicologists, pathologists, veterinarians, veterinary technicians,… more
- Pfizer (Collegeville, PA)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... the clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. + The specific components of safety data… more
- Pfizer (Collegeville, PA)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... the clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. + The specific components of safety data… more
- Merck (North Wales, PA)
- …while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be… more