- Regeneron Pharmaceuticals (Cambridge, MA)
- …Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency ... Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study...wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine how individual ... Team for a given product. May lead the Development Sub Teams or study teams and represents Clinical Science on the Global (US/EU/Japan) Development Team to… more
- Alaka'ina Foundation Family of Companies (Frederick, MD)
- …Inspector General as required. + Support 1-3 Non-human Primate studies , 40-50 rodent studies per year. Shall coordinate all study activities with study ... as needed. + CONUS/OCONUS travel may be required in support of approved studies and/or presentation of scientific research. + Prepare and participate in BSL-2 and… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Study Medical Director, Clinical Sciences is responsible for facilitating assigned ovarian and/or rare cancer studies , providing investigator support of ... may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into...role may be clinical subject matter expert for assigned studies . **A typical day in the life of a… more
- Takeda Pharmaceuticals (Boston, MA)
- …data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/site identification, enrollment strategy and ... intelligence platforms/tools to develop benchmark assumptions that enable data-driven program/ study timeline projections, country and site identification, and robust… more
- University of Colorado (Aurora, CO)
- …including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently perform study ... + Assist with and oversee the day-to-day operations of clinical trials and studies + Perform informed consent process or ensures that the informed consent process… more
- University of Colorado (Aurora, CO)
- …but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies . + Independently perform study -related ... retention. + Serve as a resource and participate in study initiation and close-out duties. + Oversee and provide...initiatives. + Act as a Primary Coordinator on multiple trials/ studies . + Assist and train junior team members. **Work… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …of plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency ... timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard… more
- Dartmouth Health (Lebanon, NH)
- … studies . * Conducts protocol reviews to assess the feasibility of potential studies . * Participates in study site selection activities. * Designs, develops ... and other appointments. * Independently executes all aspects of the study operations (subject management/regulatory) with minimal oversight from the investigator or… more
- Takeda Pharmaceuticals (Boston, MA)
- …and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine how individual ... monitoring and interpreting data from ongoing internal and external studies , assessing the medical and scientific implications and making recommendations… more
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