- Bristol Myers Squibb (Seattle, WA)
- … regulatory authoring, and life-cycle support through pivotal process development and manufacturing + Optimize downstream unit operations and support clinical ... efforts eg upstream process development , high-throughput process development + Support research -to- development transition endeavors, including… more
- Truist (Charlotte, NC)
- …description:** Manage a team of quantitative analysts focused on model development efforts specific to retail credit risk estimation methodologies. Responsible for ... the end-to-end development life cycle of quantitative models related to the...Corporate Model Risk Management, Corporate Audit, and regulators). Support regulatory examinations and address respective requests. 7. Identify, recruit,… more
- Truist (Atlanta, GA)
- …review the following job description:** Focus on aspects of model development specific to finance and risk measurement estimation methodologies. Responsible for ... aspects of the development life cycle of quantitative models. Assist with identifying and escalating model risks. Develops awareness of key partnerships specific to… more
- Gilead Sciences, Inc. (Foster City, CA)
- …possible, together. **Job Description** **Associate Director, Process Technologies and Development ** Gilead Sciences, Inc. is a research -based biopharmaceutical ... member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we… more
- Bristol Myers Squibb (Brisbane, CA)
- …and edit clinical narratives and other study-related documents. + Support the development of site and Clinical Research Associate (CRA) training materials. ... necessary to design and deliver clinical studies and programs in early clinical development . The focus will be on hematology, oncology and cellular therapies. +… more
- University of Southern California (Los Angeles, CA)
- …knowledge of regulatory Data Standards (eg, CDISC/ADaM). Knowledge of clinical research regulatory requirements (eg, Good Clinical Practice [ICH / GCP], FDA ... USC, you will be a part of a world-class research university and a member of the "Trojan Family,"...assist with statistical plans and power analysis for proposal development Successful candidates for this position will have demonstrated… more
- Stanford University (Stanford, CA)
- …a large portfolio of early-stage Catalyst healthcare Projects, guiding them from research and development through to clinical and commercial translation ("bench ... Director of Project Development and Translation **School of Medicine, Stanford, California,...focus on successful Catalyst Project translation beyond the Stanford research environment, they develop multi-year business plans and pilot… more
- Boehringer Ingelheim (St. Joseph, MO)
- …products. Responsible for both technical and communication roles for his/her function on Research & Development (R&D) new biological project core teams. Provide ... early development guidance to Research projects. Identify and...in cross departmental project teams when assigned **Requirements** + PhD from an accredited institution with two (2) years… more
- Sanofi Group (Morristown, NJ)
- … Regulatory Affairs, Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development Groups. + External contacts: Investigators, Clinical ... focus of this role is the path from the research phase through early clinical development including...Regulatory Affairs, Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development Groups. + External contacts:… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …closely with physician-scientists, clinical leads, clinical pharmacologists, BST, discovery research scientists, regulatory , non-clinical and other functions to ... leadership for the progression of the program from discovery research through development and contribute as a...documents, CDP, clinical protocols, ICFs and documents submitted to Regulatory Agencies. + Support Business Development efforts… more
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