- Daiichi Sankyo, Inc. (Bernards, NJ)
- …SummaryThe Study Delivery Lead (SDL) leads the cross functional core and extended clinical study team in end-to end delivery of the clinical trial ... insourcing. This includes global operational execution and delivery of clinical studies across multiple geographic regions, in...at the study level with responsibility for clinical study plans and execution (from planning… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. SummaryAssist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …ensure compliance with Daiichi Sankyo's quality measures. Analyze CRO performance trends within a clinical study or across several studies and resolve or ... and implement appropriate innovative and best-in-class procedures and SOP's related to clinical study oversight and execution.Ensure their direct reports are… more
- Insmed Incorporated (San Diego, CA)
- …You'll Do: Participate in cross functional teams to develop and implement clinical studies within clinical program(s). Responsibilities include but ... organizations (CROs), and external vendors to prepare, review and finalize clinical study documents and plans Contribute to scientific and operational aspects… more
- Aequor (Basking Ridge, NJ)
- Duties: Participate in study team meeting, align with study details and collaborate in meeting study objective, Provide supporting information to the teams, ... in particular RA, RACMC, Clinical ops, and GPMs. Design packaging requirements; based on...supply forecast for packaging and labeling operations. Support patient study needs that consider enrollment rates, country logistics for… more
- Merck & Co. (San Francisco, CA)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, and publicationsParticipating in internal and joint ... and drug development (at least 5 years)Demonstrated success in overseeing clinical studies and protocolsDemonstrated record of scientific scholarship and… more
- Merck & Co. (Rahway, NJ)
- …manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal and joint… more
- Merck & Co. (North Wales, PA)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal and joint ... Supervise the activities of Clinical Scientists in the execution of clinical studies .Work closely with a cross-functional group of experts in… more
- Insmed Incorporated (NJ)
- …quality, cost, and timeline parameters.Effectively manages and/or assists with cross-functional clinical study team and team members to achieve deliverables ... by demonstrating leadership competencies.Works collaboratively with Clinical Scientist, Clinical Indication/Development Lead, and clinical study team… more
- Merck & Co. (North Wales, PA)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint ... Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in… more
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