- Bristol Myers Squibb (Altoona, PA)
- …+ Creates demand for BMS medicines by articulating in a balanced manner the clinical and scientific rationale for use of products in appropriate patients. + Engages ... HCP / nurse. + Ability to communicate scientific or clinical data accurately and convincingly to help physicians best...For more on benefits, please visit our BMS Careers site . Eligibility for specific benefits listed in our careers… more
- Teva Pharmaceuticals (West Chester, PA)
- …enable high-quality, efficient, and compliant outputs for regulatory submissions and clinical trial reporting. + Lead and develop global programming teams, including ... vendors + Partner with cross-functional stakeholders (Statistics, Data Management, Clinical Development, Regulatory) to ensure alignment and successful execution of… more
- Teva Pharmaceuticals (West Chester, PA)
- …tools and dashboards and exploratory analytics to provide insights into our clinical trial data and to support decision-making across clinical development ... data visualization strategy, driving cross-functional alignment with R&D functions, Clinical Teams, Statisticians and Statistical Programming to deliver visualization… more
- Surgery Care Affiliates (Newtown, PA)
- …do it. Each decision we make is rooted in seven core values: + Clinical quality + Integrity + Service excellence + Teamwork + Accountability + Continuous improvement ... goal execution of one SCAH facility. Key Roles: * Clinical Quality and Patient Safety: Champion SCAH's HRO Journey...where the structure may evolve rapidly * Serves as on- site personnel director and ensures fair and prompt resolution… more
- Merck (North Wales, PA)
- …programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects. + Develop and execute statistical analysis ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck (West Point, PA)
- **Job Description** The PDMB Bioanalytics group at our West Point, PA site is dedicated to regulated pharmacokinetic (PK), immunogenicity, and molecular assay ... development of small molecules, vaccines, and biotherapeutics. We conduct GLP and clinical sample analysis with a commitment to scientific excellence and regulatory… more
- Merck (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Highmark Health (Pittsburgh, PA)
- …system + MS Lead is responsible for day to day operations at the site and is accountable for clinical , professional, administrative, education, research and ... category protected by applicable federal, state, or local law. We endeavor to make this site accessible to any and all users. If you would like to contact us… more
- Penn Medicine (Philadelphia, PA)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... with a collaborative and multi-disciplinary practice model. The high acuity clinical practice setting is dynamic, fast-paced, and high pressure. Excellent critical… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …our ability to plan and execute the production of commercial and late-stage clinical products efficiently, timely, and with high quality. Scope of the role covers ... of the role will be CI of Commercial or clinical products. The role will provide coaching, direction and...direct reports and will work very closely with the Site GM's and Site CI directors across… more