- Merck (West Point, PA)
- …GLP-toxicity studies . Our clinical pathologists provide scientific leadership in study design and execution, as well as complete interpretations and reports for ... studies throughout drug development. Working collaboratively across the organization,...**Key responsibilities for this scientific role include:** + **Review study protocol designs** and make recommendations regarding clinical pathology… more
- Commonwealth of Pennsylvania (PA)
- …options. Work/Life Balance We know there's more to life than just work! Our generous paid leave benefits include paid vacation, paid sick leave, eight weeks ... of paid parental leave, military leave, and paid time off for most major US holidays, as...Yes 04 COLLEGE COURSEWORK - GERONTOLOGY Defined as the study of the aging process, older adults, and the… more
- Bristol Myers Squibb (Philadelphia, PA)
- …Clinical Trial Activities** + Support Interventional and Non-Interventional Research (NIR) studies (eg identification and assessment of potential study sites) ... office medical and Global Development Operations (GDO) and as defined by the study scope document + Provide recommendations and insights to clinical development team… more
- Pfizer (Collegeville, PA)
- …proof of mechanism (POM), early signals of efficacy (ESOE) and proof of concept (POC) studies . You will also be mentored/obtain guidance from a more senior study ... of the clinical protocol and may participate as an individual contributor on clinical study teams and clinical subteams to meet enrollment and study delivery… more
- Merck (North Wales, PA)
- …Works with the Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets. + Supports affiliates to ... and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and… more
- Merck (Harrisburg, PA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial… more
- Merck (North Wales, PA)
- …will manage the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. ... cardiovascular and respiratory drugs + Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new… more
- Pfizer (Collegeville, PA)
- …input and leadership to cross-functional activities - collaborate with other statisticians, study managers, programmers - for assigned studies and regulatory ... successful candidate will collaborate closely with cross-functional project and study teams, offering statistical expertise in designing clinical trials, developing… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …configured to hold a single product, or multiple products as determined by study requirements. We offer manual patient kit assembly along with semi-automated and ... automated wallet sealing and high-speed automated carding to meet the needs of studies of all sizes. For temperature sensitive products and those with minimal to… more
- Merck (Upper Gwynedd, PA)
- …will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. ... Director may be responsible for: Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug… more