- 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …leader accountable for operational planning and execution of FIH, clin pharm patient studies , and Phases 1-3 clinical trials at the study and program level. ... or Senior Director, Clinical Operations on plans for successful implementation of studies . Responsible for management of compounds at the program and franchise… 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 ... clinical trial execution in all its aspects across all studies & phases in scope of GCTO within the...all cluster/country level GCTO team & all programs and studies .Approved administrative budget to support GCTO team (eg, salaries… 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. (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
- 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 ... reporting, and external data acquisition and validation deliverables for all studies consistent with IDRP, study data listings, exception data listings, sample… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Job Summary: Position leads complex studies in study design, statistical analysis and interpretation of results with some ... and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis… 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...and oversight of all high priority programs - and studies . Adhere to our company's standards and R&D/ GCD… more
- Merck & Co. (Rahway, NJ)
- …of this role. This position may have people management responsibility.Types of studies executed include prospective and retrospective observational studies to ... programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case report forms,… 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
- 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)
- …the candidate's pharmacology expertise, involvement in outsourcing of in vivo pharmacology studies is also a possibility; including, but not limited to, the design, ... Cardiometabolic, Communication, Genetic Research, Immunology, Infectious Disease, In Vivo Studies , Molecular Biology, Mouse Genetics, Neuroscience, Oncology, Partner Relationship… more
- Merck & Co. (North Wales, PA)
- …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… more
- Novo Nordisk Inc. (San Francisco, CA)
- …with trial/study investigation sites; ensuring effective coordination and facilitation of studies to ensure timely review, initiation, and completion, as well as ... Nordisk groups to ensure investigators demonstrate appropriate knowledge of studies , support patient recruitment and retention activities, answers responsive… more
- Tris Pharma (Monmouth Junction, NJ)
- …products (FP) and stability (ST) samples and executes physical characterization studies to facilitate product understanding. The incumbent also performs other lab ... measurementsPerforms all necessary calculations associated with test analysesExecutes designed studies to support laboratory investigationsPerforms non-routine testing such as… more
- Merck & Co. (Rahway, NJ)
- …for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. -Our development teams ensure robust composition, primary ... tools to drug product development, and experience in designing appropriate DOE studies to inform on risks.Experience with process scale-up, definition of critical… 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 ... Public Health.Research background in the design and implementation of clinical studies , familiarity with biostatistics, and/or regulatory review process is desirable… more
- Twist BioScience (South San Francisco, CA)
- …the creation of high-quality content (blogs, articles, white papers, case studies , etc.) that educates target audiences, showcases Twist's thought leadership, and ... of internal and external needs including event tactics, webinars, case studies , and training materialsDevelop a comprehensive communications process and plan for… more
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