- Merck & Co. (Rahway, NJ)
- …function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and ... candidate be responsible for the conduct of Good Clinical Practice (GCP) studies , and occasionally Good Laboratory Practice (GLP) studies .The Associate Principal… more
- Merck & Co. (Boston, MA)
- …manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, analysis, ... or marketed Atherosclerosis drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as… more
- Merck & Co. (Rahway, NJ)
- …for investigational or marketed medicinesAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as ... in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert… more
- Merck & Co. (Rahway, NJ)
- …GCP, local and global policies and procedures to conduct high-quality, inspection ready studies is essential. The position is accountable for trial quality and audit ... contact for managing clinical trial execution in all its aspects across all studies & phases in scope of GCTO within the country/clusterLeadership and oversight of… more
- Merck & Co. (South San Francisco, CA)
- …executing all phases/aspects of toxicokinetics support of nonclinical toxicity studies [ie, exploratory and definitive/Good Laboratory Practice (GLP)], serving as ... a contributing scientist/principal investigator on toxicity studies , and executing PK/TK strategies to support the development of small molecules and biologics.The… more
- Twist BioScience (South San Francisco, CA)
- …variety of internal and external needs including event tactics, webinars, case studies , and training materialsDevelop a comprehensive communications process and ... the creation of high-quality content (blogs, articles, white papers, case studies , etc.) that educates target audiences, showcases Twist's thought leadership, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …that adhere to programming standards and specifications across clinical studies . This position involves managing direct reports and/or leading multidisciplinary ... internal and external systems, CROs, and vendors. Excellent verbal/written communication , analytical, organizational, and interpersonal skills are essential for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …units, regions, and functional areas to ensure successful outcomes for projects/ studies . This position has sufficient understanding of regulations and GCP ... requirements. This position has advanced experience working on Phase I-IV studies within the pharmaceutical industry across multiple therapeutic areas and is… more
- Eisai, Inc (Nutley, NJ)
- …execution within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory ... activities directly impact the timeliness, quality, and successful execution of clinical studies in accordance with the overarching project plans established by the… more
- Merck & Co. (Rahway, NJ)
- …(LCEs) of an interventional nature and Clinical Research Organization (CRO) run studies . Adherence to Good Clinical Practice (GCP), local and global policies and ... procedures to conduct high-quality, inspection ready studies is essential. The position is responsible for trial quality and audit responses and completion of… more
- Merck & Co. (San Diego, CA)
- …successful candidate will lead projects from discovery to start of IND-enabling studies , with focus on antibodies, bispecific molecules, and evaluation of novel ... analyze new cellular and molecular assays to support mechanism-of-action studies for therapeutic candidate progression.Hands-on development of experiments related… more
- Eisai, Inc (NJ)
- …boards, real-world evidence and data generation, and scientific communication /publications. The Medical Director will utilize expert medical/scientific knowledge ... for approval of medical and scientific content of relevant materials/ communications . Responsibilities: Develop and continually refine the medical strategy based… more
- Merck & Co. (New York, NY)
- …approved, in-development, and active company-sponsored trials and/or investigator-sponsored research studies - The Regional Medical Scientific Director serves as a ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.… more
- Merck & Co. (Boston, MA)
- …Communication , Genetic Research, Immunology, Infectious Disease, In Vivo Studies , Molecular Biology, Mouse Genetics, Neuroscience, Oncology, Partner Relationship ... broad experimental capabilities and a strong work ethic, have excellent communication skills, and work effectively in a highly collaborative, cross-functional team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will collaborate ... global functions as needed; proactively identify and resolve any technical, communication , and administrative issues. Help to improve and ensure consistency, where… more
- Eisai, Inc (MD)
- …and clinical information about Eisai's products; serve as a conduit for communication between Eisai Research and the medical community regarding ideas for future ... Research Support Facilitate review and follow up of submitted Investigator-Initiated Studies (IISs) and assist with Eisai sponsored trials.Serve as primary contact… more
- Merck & Co. (South San Francisco, CA)
- …to enable strategies for assay development, screening, and mechanism of action studies to advance a diverse portfolio of therapies for cardiometabolic disorders and ... oncology. We value transparent communication , creative thinking, teamwork, and rigorous scientific exploration. If you are a highly motivated individual and team… more
- Merck & Co. (Rahway, NJ)
- …responsible for protocol development and medical/scientific oversight of clinical research studies involving new or marketed drugs in the Vaccines Clinical Research ... the ability to function in a multidisciplinary team environment Excellent communication and writing skills Strong analytical skills Prior pharmaceutical industry… more
- Merck & Co. (Rahway, NJ)
- …plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have demonstrated ... and ensures proper allocation of drug product as needed across studies within assigned program(s).-Responsible for identifying significant supply risks associated… more
- Merck & Co. (Rahway, NJ)
- …plans associated with the downstream activities of clinical supplies for their assigned studies .- The primary function of the IM CSPM is planning the availability of ... technological tools in the planning and managing of clinical supplies for assigned studies such as IRT & Microsoft PowerApps.--Works directly in the SAP system to… more
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