- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …disorders. **Job Summary:** The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy, design, ... execution, and interpretation of Oncology clinical trials. **Position Summary / Objective** + Serves as...responsibilities across the internal and external network + Manages Phase 1 - Phase 3 studies (depending… more
- Actalent (Boston, MA)
- …of work creation, and ensure compliance with quality measures and timelines. + Monitor clinical trial performance and quality metrics, escalating issues and ... procedures for planning, conduct, close out, and reporting. + Monitor and reconcile study budgets, reviewing vendor invoices and... clinical research, clinical operations, and clinical trial management. + Experience with Phase … more
- Taiho Oncology (Princeton, NJ)
- …for leading global development program(s), including strategy, design, oversight, and analysis of Phase 1-4 oncology clinical trials. This position will be the ... for global Phase I-III and "ancillary" trials as Lead medical monitor for global development program(s) + Use medical/scientific expertise and strategic thinking… more
- University of Pennsylvania (Philadelphia, PA)
- …(ie multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I - IV clinical trials and biospecimen and data ... (ie multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I - IV clinical trials and biospecimen and data… more
- Actalent (San Francisco, CA)
- … Trial Manager experience with at least 2-3 years at a Sponsor. + Experience in Phase 2/ Phase 3 clinical trials. + Experience in CNS and Alzheimer's trials. ... in Alzheimer's clinical trials. + 3-5 years of recent experience in global phase II/III clinical trials. + Experience managing clinical trials from the… more
- Sumitomo Pharma (Lincoln, NE)
- …lead the design of clinical studies in close collaboration with the Clinical Research Team. + Monitor protocol compliance including assessment of inclusion ... motivated, and experienced individual for the position of **Senior Clinical Research Scientist.** This is an exciting opportunity to...+ Comprehensive understanding of the drug development process from Phase 1 to Phase 3. + Prior… more
- Amgen (Thousand Oaks, CA)
- …sponsored clinical research is desirable + Biopharmaceutical experience as a medical monitor and clinical lead across therapeutic areas is desirable + Solid ... lives of patients while transforming your career. **Executive Director, Clinical Development, Rare Disease** **Live** **What you will do**...drug development activities from the design and execution of Phase 2 through Phase 4 studies. They… more
- Lilly (IN)
- …Planning + Collaborate with the business unit geographical regions, Discovery, Program Phase Medicine, and Clinical Pharmacology in the development and ... around the world. Through the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Development Clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …(ie, multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I - IV clinical trials and registries within the ... concert with investigators, detailed documentation of study activities). + Monitor subjects per protocol requirements and ensure adherence to...budget preparation for trials as needed. May support a clinical trial budget through each phase of… more
- Organon & Co. (Sacramento, CA)
- …plans. The Clinical Pharmacology Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction with the TMED ... the US + There are **2 openings** The Director, Clinical Pharmacology Lead will be responsible for contributing and/or...responsible for the rationale, study design and oversight of phase 1 to 2a study protocols, in collaboration with… more