- Merck & Co. (Rahway, NJ)
- Job Description Job Description: - The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & ... of our company. - Position Description/Summary: - The GPAM Associate Director, Project Manager, is a core member of...Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams,… more
- Merck & Co. (South San Francisco, CA)
- …who can independently design and execute mathematical modeling approaches to inform drug discovery, with minimal supervision. Associate Directors work with ... & Bioanalytics (PDMB) is seeking a curious and collaborative Scientific Associate Director for our growing Translational PK/PD organization. The Translational PK/PD… more
- Merck & Co. (Rahway, NJ)
- …on drug /vaccine development programs, and author or co-author strategic documents. Associate Directors are expected to have or be developing expertise in several ... DescriptionThe Quantitative Pharmacology and Pharmacometrics (QP2) department drive model-informed drug discovery and development (MIDD) to routinely enable efficient… more
- Aequor (Bothell, WA)
- …submit candidates previously viewed by manager) Position Summary: The Inventory Control Associate will be responsible for performing hands-on operations in the areas ... material, receiving, inspection, storage, transferring and issuing inventory of materials, drug substance in intermediates, governed by SOP's. The Inventory Control … more
- Aequor (Thousand Oaks, CA)
- …join our Pivotal Drug Product Technologies Group as Process Development Senior Associate in Thousand Oaks, CA. This group is responsible for late-stage drug ... monoclonal antibodies, bispecific T-cell engagers (BiTEs), fusion proteins, etc.). The Senior Associate will work in a highly collaborative team focusing on high… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on ... Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution...with internal Functions within the study team to ensure drug destruction process and other study close out activities… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology evaluation and ... focus on front-end development, emphasizing the exploration and assessment of emerging drug delivery device technologies. The ideal candidate will lead efforts in… more
- Merck & Co. (North Wales, PA)
- …and maintaining programs in harmony with the portfolio . In addition, the Associate Director will be expected to participate in development of tools and processes ... Clinical strategies . - Position Description/Summary: - The CIPM Associate Director, Project Manager , is a core member...lead s to develop strategies and execute our Company's drug and vaccine development efforts to progress the R&D… more
- Genmab (NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development of ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
- Merck & Co. (Boston, MA)
- …Bioanalytics (PDMB) group is seeking a dynamic, strategic thinking and collaborative Associate Principal Scientist to contribute to our small molecule and peptide ... drug discovery and early clinical development efforts. -This position...labs in Boston, MA.- The ideal candidate will lead drug metabolism and pharmacokinetic (DMPK) efforts as a project-team… more
- Aequor (South San Francisco, CA)
- Job Title : Research Associate II Location : South San Francisco, CA Duration : Until 01/12/2026 Job Description: The mission of the Investigative Toxicology group ... support the overall safety assessment for our Client therapeutics spanning drug discovery through clinical development and marketing. The group provides… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Batch Disposition Associate Manager as part of the Quality team based in Raritan, NJ. Role ... wide range of activities to support the release of drug products for human use. This position is responsible...all applicable regulations.Key Responsibilities Manage the team responsible for drug product batch record review and drug … more
- Genmab (NJ)
- …our best, and authentic is essential to fulfilling our purpose.The Role:An Associate Director, Data Management is operationally responsible for the oversight of ... delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight to ensure end-to-end data management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing ... provide scientific and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of BLA/MAA… more
- Merck & Co. (Rahway, NJ)
- …Modeling Team in our Company Manufacturing Division seeks an experienced Associate Principal Scientist who will develop and utilize advanced computational models ... role, you will build and apply predictive tools for drug substance (upstream, downstream, and conjugation) and drug... drug substance (upstream, downstream, and conjugation) and drug product manufacturing unit operations using a variety of… more
- Aequor (Devers, TX)
- Bio-Process Associate , 2nd Shift6 Months Contract - With high possibilities of extension100% Onsite in Devens, MA Please refer to the attached Work Schedule Shift ... of a vehicle or machinery, or physical presence in a laboratory, research, drug development, or manufacturing facility are prohibited from having any amount of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical ... Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Respiratory will focus on driving strategy, development, and life-cycle ... understanding of the disease area, the functions and processes relevant to drug development, and project management principles as applicable to the pharmaceutical… more
- Aequor (Thousand Oaks, CA)
- …The Sr. Associate will also represent functional area for the Drug Substance Quality Assurance department in the execution of projects necessary to achieve ... program under the Plant QA organization providing daily oversight of the Drug Substance manufacturing areas. Under general supervision, the role provides support and… more
- Merck & Co. (Rahway, NJ)
- …& Process Development (DPPD) Team designs, develops, and commercializes novel biologic/ drug /vaccine - device enabled combination products to achieve safe and ... set direction for the device development strategy for multiple drug -device combination product development programs ranging from concept generation/selection,… more
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