- Merck (West Point, PA)
- …esteemed scientific leader in the process development and manufacturing of vaccine drug substances for the role of Distinguished Scientist (equivalent to the ... substances (DS) and adjuvant bulk for the entire vaccine pipeline at our company, spanning from preclinical to...Scientist to lead our VAX PR&D team in drug substance (DS) process development and manufacturing. In this… more
- Merck (North Wales, PA)
- …and modular analysis and reporting and submission standards that can be used for drug and/or vaccine projects across all therapeutic areas. + Adheres to standard ... of statistics, clinical trial, and data management concepts as applied to drug / vaccine development. + Expertise in applying SAS for clinical trial programming… more
- Merck (North Wales, PA)
- …Activities:** Provide support to statistical programming activities for late-stage drug / vaccine clinical development projects. Develop and execute statistical ... analysis and reporting deliverables (eg, safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. Design and maintain… more
- Merck (Lower Gwynedd, PA)
- …developing and expanding your career. We are seeking a highly motivated Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalysis ... handling. The successful candidate will contribute under guidance of a senior team member to the bioanalytical assay development, optimization, validation, and… more
- Merck (North Wales, PA)
- …data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly ... **Position Specific Required Skills and Experience:** + US and/or worldwide drug or vaccine regulatory application submission experience including the… more