- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Associate Director will be responsible for developing and implementing Clinical Pharmacology and Modeling & Simulation plans from FIH to post registration. ... Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design and lead...plans, design and lead study teams to execute Clinical Pharmacology studies, conduct hands on population PK and PKPD… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …development plan, design, conduct, and interpret Phase 1 (specifically Clinical Pharmacology ) studies, support Phase 2/3 studies, represent function on study and ... management, and outside vendors.ResponsibilitiesResponsible for all aspects of Clinical Pharmacology and Biopharmaceutics studies and model-based drug development plans,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …diseases and immune disorders. Summary The Associate Director, Quantitative Systems Pharmacology (QSP) will work within the Quantitative Clinical Pharmacology ... of QSP within Oncology/Immuno-Oncology. ResponsibilitiesDevelop and apply Quantitative Systems Pharmacology (QSP) models to address drug-discovery and development questionsDevelop… more
- Merck & Co. (Rahway, NJ)
- …We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate ... and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.Associate… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Quantitative Pharmacology and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable ... and regulatory decisions Deep knowledge of drug development, pharmacokinetics and pharmacology and basic science skills required. - Preferred Experience and skills:… more
- Merck & Co. (Boston, MA)
- …innovative Associate Principal Scientist with a strong background in In Vitro Pharmacology to join the External Quantitative Biosciences group (ExQB).Under the broad ... A Bachelor's Degree (BA/BS) in Biochemistry, Biophysics, Enzymology, Protein sciences, Cell pharmacology , molecular biology or a relevant In Vitro Pharmacology … more
- Insmed Incorporated (Bridgewater, NJ)
- …project teams, strategize nonclinical safety data package, oversee safety pharmacology and toxicology studies, author nonclinical sections in regulatory submission ... oligonucleotides, and/or gene therapies is a plus. Advanced knowledge of toxicology, pharmacology , safety pharmacology & DMPK. Comprehensive knowledge of GLP… more
- Merck & Co. (Boston, MA)
- …determining and implementing the initial clinical strategy through proof-of-concept/ pharmacology / principle and the transition from early to late-stage ... governance.-In addition, the AVP's responsibility will include the clinical pharmacology support of the Common Technical Document (CTD) and label, including relevant… more
- Merck & Co. (Rahway, NJ)
- …determining and implementing the initial clinical strategy through proof-of-concept/ pharmacology /principle and the transition from early to late-stage governance.-In ... addition, responsibility will include the clinical pharmacology support of the Common Technical Document (CTD) and...DRC reviews (protocols, strategy, other) Sign off on clinical pharmacology CTD submissions and NDAs Regular updates with key… more
- George Washington University (Washington, DC)
- I. DEPARTMENT INFORMATION Job Description Summary: The Department of Pharmacology & Physiology at the George Washington University is an active research department, ... with federally funded programs in neuroscience and development, cardiovascular pharmacology and integrative physiology, genomics and oncology. We provide unique… more
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