- Merck (West Point, PA)
- …future for all. We have an exciting opportunity for an ** Associate ** ** Principal Scientist ** with experience in Vaccine biology or Immunology to ... join our Quantitative Biosciences team in West Point, PA. Working collaboratively with our local discovery teams the successful candidate will apply their skills in assay development, data analysis, laboratory automation and assay detection technologies to… more
- Merck (West Point, PA)
- …Product Development (VDPD), a part of our company's Research Laboratories, is seeking an Associate Principal Scientist to join our department in West Point, ... PA. Our mission is to develop novel vaccine drug products that will profoundly improve global human...to eliminate disease. Our department is responsible for developing vaccine adjuvants and drug products from preclinical studies through… more
- Merck (Lower Gwynedd, PA)
- …while developing and expanding your career. We are seeking a highly motivated Associate Principal Scientist to join the Department of Pharmacokinetics, ... vaccines pipeline. The individual will be responsible to lead vaccine bioanalytical assay development, qualification/validation, technology transfer, and/or troubleshooting… more
- Merck (North Wales, PA)
- …coordinates, and provides biostatistical leadership and support for related drug/ vaccine projects in Late Development Statistics. + Interacts with Clinical, ... clinical trials, and in coordinating the statistical activities for clinical drug/ vaccine projects. May interact with Contract Research Organization (CRO). + This… more
- Merck (North Wales, PA)
- …statistical programming activities for multiple and/or late stage drug/ vaccine clinical development projects. Accountability predominantly includes the development ... activities of a programming team. + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the… more
- Merck (North Wales, PA)
- …with Meta Data Repositories. + United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the ... development of CRT SDTM study data standard deliverables. + Strong knowledge of study data standards. + Up-versioning activities to specific versions of Statistical Analysis System (SDTM). + Participation in industry teams and conferences on best practices. +… more