- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diseases and immune disorders. Job Summary: Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... appropriate.Participate in training; make recommendations for areas of improvement and innovation ( study , or departmental level). Work with supervisor to provide… more
- Merck & Co. (Rahway, NJ)
- …Practice (GLP) studies .The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study .The Associate ... function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …clin pharm patient studies , and Phases 1-3 clinical trials at the study and program level. Responsible for clinical program planning and execution (from study ... implement appropriate innovative and best-in-class procedures and SOP's related to clinical study oversight and execution. Work with TMF Operations to ensure a… 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 ... touch points across the company which will be dependent on country/cluster and the study type and stage.ED is the primary country/ cluster level contact for GCTO and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …programming, reporting, and external data acquisition and validation deliverables for all studies consistent with IDRP, study data listings, exception data ... delivery of programming deliverables, including integrated data review plan (IDRP), study data listings and exception reports, sample data reconciliation, external… more
- Merck & Co. (South San Francisco, CA)
- …to the following: conduct TK modeling to support dose-selection on toxicity studies , provide TK study design, calculate PK/TK parameters, interpret results, ... quality scientific results according to agreed timeline for several concurrent studies .Effectively communicate study results at internal meetings, as… more
- Eisai, Inc (Nutley, NJ)
- …As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, ... execution within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory… more
- Merck & Co. (Boston, MA)
- …will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... May: Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in… more
- Merck & Co. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... of this role. This position may have people management responsibility.Types of studies executed include prospective and retrospective observational studies to… 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...are met for all trials executed in the region. Work collaboratively in a matrix organization with all groups… more
- Merck & Co. (New York, NY)
- …to scientific questions from SLs, including questions about company products - The work of a Regional Medical Scientific Director is aligned to: Scientific Exchange, ... approved, in-development, and active company-sponsored trials and/or investigator-sponsored research studies - The Regional Medical Scientific Director serves as a… more
- Eisai, Inc (Nutley, NJ)
- …the clinical, project management, and data manager teams on strategic designs of studies ; develops, reviews and/or approves study documents such as clinical ... As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile,… more
- Merck & Co. (North Wales, PA)
- …to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, ... approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The Regional Medical Scientific Director serves as a… more
- Eisai, Inc (Nutley, NJ)
- …Proficient in MS outlook, word, power point and excelBasic understanding of study related documentationseTMF (Veeva) experience preferredAbility to work with ... As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile,… more
- Genmab (NJ)
- …and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of ... and development of data-driven early indication and program assessments, study -level feasibility assessments, robust country and site identification, support of… more
- Novo Nordisk Inc. (San Francisco, CA)
- …products and development activities in the medical community Collaborates with trial/ study investigation sites; ensuring effective coordination and facilitation of ... studies to ensure timely review, initiation, and completion, as well as publication of study results. Provides clinical support in cooperation with other Novo… more
- Eisai, Inc (NJ)
- …As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, ... users are effectively utilizing the eTMF system for active and archived studies . This includes overseeing the daily global eTMF system related activities relating… more
- Genmab (NJ)
- …within a study are in scope. The Programming Manager will work with other functions including Data Management, Statistics, Drug Safety, Medical, Clinical ... best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have...consistency and/or adherence to standardsParticipates in review of key study documents, including but not limited to SAP and… more
- Aequor (Athens, GA)
- …In addition, this individual conducts scientific procedures in accordance with study protocols, completes and maintains appropriate documentation associated with all ... and provides equipment sanitation and facility maintenance. This individual will work in a research laboratory setting under Biosafety Level 2 conditions.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …TLFs generated by statistical vendor, ensure deliverable quality for the pivotal studies , Integrated Summary of Efficacy (ISE)/Integrated Summary of Safety (ISS) for ... submissions. Responsibilities include: review Case Report Form (CRF) annotation and Study Date Tabulation Model (SDTM) dataset, identify data inconsistencies and… more
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