- Sanofi Group (Cambridge, MA)
- …The role of the Senior CRD is to: + Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs ... and prepare/assist with regulatory bodies interaction + Develop the study level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol) for… more
- Sanofi Group (Morristown, NJ)
- …prepare/assist with regulatory bodies interaction + Provide clinical scientific expertise in the Study team to conduct the clinical studies from early phases to ... LCM programs + Develop the study level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol)...input & support for all activities related to clinical studies conduct such as answers to IRBs and HA… more
- 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... studies and within clinical program(s) to track study progress + Provide proactive creation and implementation of… more
- University of Pennsylvania (Philadelphia, PA)
- …activities within the Cardiovascular Division of PPMC Responsible for assisting with study coordination and recruitment for industry sponsored studies . Works ... activities within the Cardiovascular Division of PPMC. Responsible for assisting with study coordination and recruitment for industry sponsored studies . Works… more
- University of Pennsylvania (Philadelphia, PA)
- …such as atopic dermatitis and psoriasis. The lab engages in quantitative epidemiologic studies ranging from survey studies to large population-based database ... and foundation sponsors. Current projects include ADDS-UP3, a community-based cohort study aimed at identifying the social and environmental factors contributing to… more
- University of Pennsylvania (Philadelphia, PA)
- …Research Coordinator (CRC) is responsible for the execution of clinical research studies as part of the Department of Orthopaedic Surgery's Clinical Research Team ... institutions and creates multi-center budgets and manages expenses. Participates in study team meetings, disease site group meetings, and ongoing protocol… more
- University of Pennsylvania (Philadelphia, PA)
- …and run several different studies . The tasks involved in these studies include recruitment of study participants including finding eligible participants ... Practice (GCP). + Assist in planning and implementation of patient recruitment into studies and screen, recruit and retain potential study participants. + Assist… more
- Guidehouse (Frederick, MD)
- …Obtain Public Trust **What You Will Do** **:** + Provide services to support animal studies , such as assist the Federal Task Leader to manage a team of technical ... clinical pathology assays and in support of animal and other research studies performed at IRF-Frederick. + Manage all clinical laboratory equipment, work with… more
- University of Colorado (Aurora, CO)
- …+ Assist with and oversee the day-to-day operations of clinical trials and studies + Obtain study subject's medical history and current medication information, ... to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently...all other essential study documents for assigned studies + Independently perform study related processes,… 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