- Eisai, Inc (Nutley, NJ)
- …work independently to complete analyses while proactively providing updates to the project team and according to timelines and requirements. The candidate should ... evidence gap assessmentContribution to product evidence generation planManagement of project vendorsContract & budget tracking Requirements A postgraduate degree… more
- Merck & Co. (South San Francisco, CA)
- …of novel respiratory medicines, from early research up to clinical development. Design and execute strategies for target identification, validation, and translational ... hypertension, NCFBE).Effectively manage and lead multiple projects, including experimental design , resource allocation, and timeline adherence, ensuring milestones are… more
- Merck & Co. (South San Francisco, CA)
- …immunology, oncology, cardiovascular and metabolic disease, and ophthalmology.Key Responsibilities: Project -team representative for biologics or other modality drug ... team strategy and lead the formation and execution of team-specific PDMB workflow. Design and execute in vitro and in vivo mechanistic and translational studies… more
- Reed Smith LLP (Pittsburgh, PA)
- …by the Business Applications Team. Performs technical analysis, architectural design , development and implementation of client/server applications and advanced ... Develop SQL Integrations and reports using MS Reporting Services. Database design , development, and data warehousing utilizing SQL. Migrate, convert, import /… more
- Merck & Co. (North Wales, PA)
- …the entire cycle of clinical development, including study design , initiation, execution,-monitoring, analysis, regulatory reporting, publication, and presentation ... requirements, the competitive landscape, and commercial considerations;Planning clinical trials ( design , operational plans, settings) based on these clinical development… more
- Merck & Co. (Boston, MA)
- …of clinical trial process (mainly Phase 2-3) including study design , medical monitoring, and medical/scientific interpretation of study analyses,-regulatory ... the Senior Principal Scientist is responsible for:Planning clinical trials ( design , operational plans) based on the clinical development strategies for… more
- Merck & Co. (Rahway, NJ)
- …clinical development and studies, including development strategy, study design , initiation, execution, monitoring, analysis, regulatory reporting, and ... strategies for investigational or marketed Atherosclerosis drugsPlanning clinical trials ( design , operational plans, settings) based on these clinical development… more
- Twist BioScience (South San Francisco, CA)
- …within the NGS portfolio.Successfully engage with advertising agencies and the internal design team to deliver high-quality assets, including, but not limited to, ... computer skills, Microsoft Office Suite and/or Gsuite; working knowledge o program/ project management software (eg, Smartsheet, MS Project )Experienced at… more
- Christus Health (Grand Prairie, TX)
- …end user conflicts. Provides clear and organized status reporting on key project areas to be used as external communications to stakeholders. Provides insight ... and agreeable way among peers. Strong technical proficiency in application-specific design and configuration. Ability to clearly articulate and communicate core … more
- Genmab (NJ)
- …the implementation of strategic, data-driven feasibility practices that optimize the design and delivery of clinical trials across Genmab's development portfolio. ... Operations (DevOps), Clinical Strategy and external partners to inform study design and operational delivery strategies.Shape feasibility approaches and standards by… more
