- Merck & Co. (North Wales, PA)
- …to meet the value evidence needs of payers, advisory committees health systems , and clinicians.The incumbent can generate these plans based on direct interactions ... and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and… 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 ... the planning and managing of clinical supplies for assigned studies such as IRT & Microsoft PowerApps. -Works directly...IRT & Microsoft PowerApps. -Works directly in the SAP system to ensure a robust and consolidated forecast for… more
- Eisai, Inc (Nutley, NJ)
- …as well as the clinical execution and oversight of the associated studies being conducted globally. The Executive Director will champion transformational business ... to conduct Phase I, Phase II and Phase III studies , and prepare related documentation for submissions.This position will...Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in… 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- …protocols, reports).Review and approve periodic review documentation for qualified equipment/ systems (audit trails, user groups, system administration)Provide ... providing quality oversight over the validation and qualification activities for equipment, systems , computer systems , and processes within a cell therapy… more
- Aequor (Thousand Oaks, CA)
- …(eg, EDC systems , data integration platforms, data flow). Participate in system design, and user acceptance testing. Role model with staff on new technologies ... Analytics to layer to the model which will deliver studies with an appropriate risk-based approach, eg. reduced SDV...o Deep knowledge of clinical data management processes and systems (eg, EDC, CDISC standards, External Data Collection, eg… more
- Novo Nordisk Inc. (Boston, MA)
- …Nordisk within a specified geographic area, engaging with selected health systems , key academic centers, specialists, primary care providers, and other stakeholders. ... Management Assess and adapt sales and promotion strategies to align with health system account practices, care pathway decisions and managed care impact in the… more
- Merck & Co. (North Wales, PA)
- …Evidence (RWE) in Oncology.- -Position objectivesTo design and execute real-world evidence studies , designed to demonstrate the value of new products in support of ... inform and contribute to the value evidence plan and associated studies which demonstrate clinical, economic, and patient-centered value. The work will… more
- Merck & Co. (Rahway, NJ)
- …review with clinical partners and senior leaders.- - Works directly in the SAP system to establish a consolidated , visible forecast for all study product needs ... non-pipeline activities. - Participate in Interactive Voice Response (IVR) System d evelopment and User Acceptance Testing (UAT) for...d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members and supports… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in overseeing the development, validation, implementation, and integration of GxP-regulated systems across the organization. This position ensures that all global ... systems , electronic records, validation processes, and regulated applications meet...current with emerging technologies and industry trends; lead feasibility studies , prototype development, and advocate for scalable, compliant architecture… more
- Merck & Co. (Rahway, NJ)
- …release of drug product across assigned program(s) . - Works directly in the SAP system to establish a consolidated , visible forecast for all product s used within ... management and ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying significant supply risks… more
- Merck & Co. (Rahway, NJ)
- …evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and ... programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case report forms,… more
- Merck & Co. (North Wales, PA)
- …payers, policymakers, health technology assessment (HTA)/reimbursement agencies and health systems globally.Types of studies executed include prospective and ... programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case report… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …will be part of Manufacturing Excellence team reporting to the Manufacturing Execution Systems Lead and will be responsible for EBR development and administration at ... This individual will support electronic batch record (EBR) updates and system improvements, support applicable process and facility updates, and support… more
- Eisai, Inc (Exton, PA)
- …supply of DS/ADI for pre-clinical and phase I to phase III clinical studies , including the development of long-range planning and weekly production schedules. Be ... produce material for toxicology and phase I to III studies ), and in the late-stage processes at CMOs that...be responsible to maintain and/or enhance the production area systems and technology to remain compliant with regulations and… more
- Eisai, Inc (Nutley, NJ)
- …and CDISC standards. The role will require excellent technical skills in SAS systems and application development and experience. The Associate Director must be a ... EDC user access reports that are use across all oncology studies by management.Develop/maintain Oncology standard macro library, standard listings, and… more
- Eisai, Inc (Minneapolis, MN)
- …Research Support Facilitate review and follow up of submitted Investigator-Initiated Studies (IISs) and assist with Eisai sponsored trials.Serve as primary contact ... scientific expertise to Investigators involved in company sponsored post-marketing studies . Professional Organization Support Lead field medical efforts in support… more
- Eisai, Inc (Nutley, NJ)
- …understand best practices for establishing diagnostic and treatment algorithmsHelp develop case studies and share with health system C-suite to encourage ... as well as emotional intelligenceIn-depth knowledge of integrated health systems operations within current market environmentDemonstrated ability to establish and… more
- Merck & Co. (Rahway, NJ)
- …brand strategies for assigned TAsProvides a solid understanding of how countries' medical systems and standards of care need to change to accept new innovation, how ... real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study programLeads… more
- Twist BioScience (South San Francisco, CA)
- …our silicon-based, massively-parallel DNA synthesis platform, you will conduct laboratory studies to develop, improve, and troubleshoot our latest NGS products. In ... and programming skills (python, R, shell scripting)Experience with liquid handling systems and automation toolsFamiliarity and/or interest in either liquid biopsy… more
Related Job Searches:
Electrical Engineer System Studies,
Power System Studies Engineer,
Senior Power System Studies,
Senior System Studies Engineer,
Social Studies System,
Sr System Studies Engineer,
Studies,
System,
System Studies Engineer