• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    … management expertise to project/study teams to optimize study-specific clinical trial processes.May participate in process improvement ... medical device, pharmaceutical company, or similar environment (eg, CRO) requiredExperience with clinical data standards requiredDaiichi Sankyo, Inc. is an equal… more
    HireLifeScience (04/30/24)
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  • Merck & Co. (Rahway, NJ)
    …and clinical outcomes assessments.2. Serves as project manager of all clinical data management activities for trials as assigned.- Under the guidance ... Job DescriptionThe Trial Manager creates and ensures the successful execution of the clinical data management strategy for assigned trials within a… more
    HireLifeScience (04/26/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and execution and reporting of all global oncology medical affairs operations clinical trial activities, ensuring adherence to timelines, budgets, project, and ... disorders. Summary Provide support for all aspects of Global Clinical Operations with a high degree of quality in...expectations. Ensure regular updates provided to Study Lead on trial metrics, data , and quality.Establish strong partnership… more
    HireLifeScience (04/18/24)
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  • DivIHN Integration Inc (San Diego, CA)
    …working with biological specimens and data sets, ideally with some clinical trial familiarity Will be providing general administrative support to the ... our Talent Specialists Sivanesan at 224 369 0756 Title: Clinical Trial Assistant (CTA) Location: San Diego,...Medical, Clinical , Scientific Organization and assistance to department Manager more
    JobGet (05/01/24)
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  • Novo Nordisk Inc. (San Antonio, TX)
    …ICH-GCP guidelines, and relevant regulatory requirements Ensure accuracy, validity and completeness of data collected at clinical trial sites in accordance ... The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data...principles to trial planning and conduct of clinical trials Demonstrates proficiency with computer skills… more
    HireLifeScience (05/03/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …and the application of those principles to trial planning and conduct of clinical trials Demonstrated computer skills (MS Office, clinical trial ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… more
    HireLifeScience (05/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …oncology, immunology, or complex disease therapeutic area is a must.Working knowledge of Clinical trial data systems and/or EDC and related applications ... party data from diverse external providers for clinical trials , companion diagnostics trials ,...optimal approaches to support the collection of diverse external data types.Advises Study Data Manager more
    HireLifeScience (04/28/24)
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  • George Washington University (Washington, DC)
    …Subcontracts, teaming agreements, Master Service Agreements and Master Clinical Trial Agreements, Material Transfer Agreements, Data Use and Data ... and negotiation for all industry supported clinical trials and clinical research. Dedicated Research Program Manager of grant and contract proposals… more
    JobGet (04/30/24)
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  • Merck & Co. (North Wales, PA)
    …management and prioritization skillsStrong analytical skills with the ability to interpret clinical trial data and synthesize conclusionsInteract with key ... team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of… more
    HireLifeScience (05/03/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …(eg, CRO); oncology, immunology, or complex disease required- 7+ years working knowledge of Clinical trial data systems and/or EDC lab management tools is ... party data from diverse external providers for clinical trials , companion diagnostics trials ,...meetings, and selection of vendors. Provide support to Study Data Manager with all invoice approvals if/when… more
    HireLifeScience (04/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …support training and ensure implementation of ADaM and TLFs standard in clinical trials analysis- Provide programming support to prepare regulatory requested ... analysis dataset and TLFs transfers for ongoing and complete trials , confirm data use and output quality,...within pharmaceutical industry, or CROs supporting statistical analysis of clinical trials programming with a masters degree… more
    HireLifeScience (05/02/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …literature review and creates reference list for study.Study Planning: Contributes to clinical trial planning including identification of potential risks to ... and protocol compliance for consistency with study strategy; reviews emerging clinical data regularly; performs quality assessment of Tables/Listings/Graphs… more
    HireLifeScience (04/10/24)
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  • Merck & Co. (Rahway, NJ)
    …and present technical information effectively.Excellent understanding and working knowledge of clinical research, phases of clinical trials , current ... and externally. Acts as primary site contact and site manager throughout all phases of a clinical ...continuity of site relationships through all phases of the trial .Performs clinical study site management/monitoring activities in… more
    HireLifeScience (05/02/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    clinical trial outsourcing, health sciences or related field ( clinical trials ) required.Advanced WORD and Excel skills preferred.Excellent time management ... the outsourcing process and procedures. (not a formal people manager ). Develops detailed bid analysis for the RD functional...skills preferred.Experience with PH.1 - PH. IV clinical trial vendor contracts required.Experience with CRO… more
    HireLifeScience (05/02/24)
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  • Merck & Co. (Ames, IA)
    …The position will require developing trial protocols, monitoring and summarizing clinical and marketing support trials specific to Ruminant animal health.- ... team takes a customer centric perspective using customer feedback and market intelligence data . Using this data , we design, develop and deploy products,… more
    HireLifeScience (04/26/24)
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  • Russell Tobin & Associates (San Diego, CA)
    …Manage assigned R&D Quality Risk Management activities - assessment of QC of clinical trials execution in a GCP regulated environment Support Drug Safety ... with internal R&D teams and Contract Service Providers as clinical trials are designed and conducted Identify...measure performance metrics, and suggest areas for improvement for clinical trial related processes and procedures Lead… more
    JobGet (04/29/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …is preferred A minimum of eight (8) years of progressively responsible clinical development/ trial experience within a pharmaceutical, biotechnology, or CRO ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at...with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR… more
    HireLifeScience (05/02/24)
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  • Aequor (Piscataway, NJ)
    …stakeholders. The S/MMC is expected to: Possess ability to understand and interpret clinical trial data , the literature and associated therapeutic conditions ... Job Title: Manager /Sr. Manager Medical Communications Hybrid schedule:...Ability to establish and leverage relationships with external experts, clinical trial investigators, journal editors, and congress… more
    HireLifeScience (04/20/24)
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  • Merck & Co. (North Wales, PA)
    …least 2 years of experience in publication managementUnderstanding of the clinical development process andclinical study data for assigned ... Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for… more
    HireLifeScience (04/25/24)
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  • Eisai, Inc (Nutley, NJ)
    …experiences, and clinical investigators and their staff regarding AE's from clinical trials . 30%Assist in projects requiring review and assessment of medical ... procedures, standardization of coding practices among International offices.Interface with Clinical for investigator training Essential Functions Adverse event information… more
    HireLifeScience (04/26/24)
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