- Merck & Co. (Rahway, NJ)
- … provide internal scientific leadership for cross-functional areas supporting clinical trials and will interact externally with key opinion leaders.Education:MD ... Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries...hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for… more
- Merck & Co. (Boston, MA)
- …provide internal scientific leadership for cross-functional areas supporting clinical trials, and will interact externally with key opinion leaders.-Specifically, ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Atherosclerosis… more
- Merck & Co. (Boston, MA)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Eisai, Inc (Nutley, NJ)
- …is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming ... for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS program development for… more
- Merck & Co. (Rahway, NJ)
- …has arisen for a Sr. Data Scientist in the Pharmaceutical Sciences and Clinical Supply (PSCS) Organization. - The role will be essential in establishing and ... of our digital transformation strategy. - Further, the successful candidate will provide centralized support and expertise to teams across Research Laboratories. -… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing,...hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials. GCS is accountable for the planning, sourcing,...hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders.Summary: The qualified candidate will provide knowledge-based coordination, authoring, and management of Dose Preparation ... Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The...Instructions Pharmacy Manual in support of the DSI portfolio. Provide strategic leadership related to HCP focused training materials;… more
- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. The Vice President/Head of Global Clinical Operations is a senior leadership role responsible for overseeing all aspects of ... clinical trial execution within a pharmaceutical or biotechnology company....management, oversight, and direction of TMF across all business functions. Provide training and oversight to employees and CROs on… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …feasibility and contributes to the site feasibility assessment from a physician's perspectiveMay provide clinical input into the eCRF (Case Report Form) design, ... Job Summary: The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy,...any time during the conduct of the study to provide medical inputProvides medical guidance for coding of AEs,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: Senior clinical operational 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. Responsible...by the CRO(s), lead the CRO selection process and provide input into ARO selection.Validate the study implementation plan… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …remediation plan.Distribute key study documents to the CRO and vendors as appropriate. Provide clinical administrative support to the study teams. This may ... diseases and immune disorders. Job Summary: Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate… more
- Novo Nordisk Inc. (San Diego, CA)
- …health centers, HCPs and other stakeholders in a given geography. Utilizing approved clinical resources to support provider efforts to deliver appropriate care ... for patients. Our goal is to provide information as a trusted advisor in care for...growth of the therapeutic market. This is not a clinical patient-facing role. Relationships The CM Educator is an… more
- Novo Nordisk Inc. (Denver, CO)
- …Sales Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg, counterparts, ... to drive performance Coordinates and collaborates with other representatives to leverage provider relationships in both Endo and PCP segments to drive results across… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Novo Nordisk Inc. (Boston, MA)
- …health centers, HCPs and other stakeholders in a given geography. Utilizing approved clinical resources to support provider efforts to deliver appropriate care ... for patients. Our goal is to provide information as a trusted advisor in care for...growth of the therapeutic market. This is not a clinical patient-facing role. Relationships The CM Educator is an… more
- Merck & Co. (Rahway, NJ)
- …Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of ... clinical development at our company's Research Laboratories. Translational Molecular...histopathology-based assays in the laboratory as part of a team. Provide subject matter of expert pathologist input to discussions… more
- Genmab (NJ)
- …and design input to ensure external data requirements are aligned with clinical and scientific objectives. Provide SME-level training on lab data management ... Director, External Data Quality Management, is a strategic leadership role within Clinical Data Management. This individual is accountable for driving the strategy,… more
- Merck & Co. (North Wales, PA)
- …: This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
