- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... and external network Manages Phase 1 - Phase 3 studies (depending on assignment) with demonstrated decision-making capabilities Provides...visits at any time during the conduct of the study to provide medical input- Provides medical guidance for… more
- Merck & Co. (Rahway, NJ)
- …dedicated colleagues while developing and expanding your career. - The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and ... a particular focus on obesity and obesity-related metabolic disorders. - The Senior Director will manage the entire cycle of clinical development, including study… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... the internal and external network, Manages Phase 1 - Phase 3 studies (depending on assignment) with demonstrated decision-making capabilities. Provides medical and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …PIs to plan study and monitor completionStudy outputs: For Phase 2 studies : Drafts responses to IRBs and HA, Collaborates with TMCP to ensure appropriate ... Project Teams, possibly as Global Clinical Lead. ResponsibilitiesStudy Strategy: Clinical study leader (CSL) or major scientific/medical contributor; For large or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Summary Position leads complex studies in study design, statistical analysis and interpretation of results ... and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development,… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director of In Vivo Pharmacology as part of the Research & Development team ... position will perform preclinical and IND-enabling in vivo pharmacology and toxicology studies to support pipeline programs. The ideal candidate will have knowledge… more
- Merck & Co. (Rahway, NJ)
- …position drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the Program Lead, you will collaborate with ... global, cross-functional team members including clinical directors and study managers to lead/support clinical trial scientific activities in the Atherosclerosis &… more
- Merck & Co. (Rahway, NJ)
- …engine that drives our Company's biopharmaceutical business.Position Description: Associate Director , Finance Clinical Development Finance (CDF) is responsible for ... individual goals.Under the guidance of the Oncology Clinical Development Finance Director , the Finance Associate Director will:Provide financial planning,… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility to lead ... monitoring and oversight of assigned clinical programs including monitoring of clinical studies , review & interpretation of clinical trial data, authoring clinical … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director , Human Factors plays a pivotal role in combination product development (both design and process), commercialization and lifecycle ... in our company's portfolio and pipeline including acquisition products.This Director position will interact extensively with all subject-matter experts within… more
- Tris Pharma (Monmouth Junction, NJ)
- Associate Director / Director , Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. ... Junction, NJ headquarters has an immediate need for an experienced Associate Director / Director , Analytical Research & Development. Job Title commensurate with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for a living. Are you ready to make a difference? The Position The Medical Director serves as the subject matter expert for our products and related data within the ... Key Opinion Leaders (KOLs), Healthcare Professionals (HCPs), and other stakeholders. The Medical Director will also assist the Senior Medical Director in the… more
- Eisai, Inc (Jersey City, NJ)
- …is your profile, we want to hear from you. Job Summary The Associate Director , Medical Writing will be the designated Lead Medical Writer for multiple Programs, ... and advanced knowledge of the compound to ensure alignment and consistency across studies . The qualified candidate will have proven ability to effectively manage the… more
- Merck & Co. (Rahway, NJ)
- …real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study ... Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and...global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) engages… more
- Novo Nordisk Inc. (Omaha, NE)
- …strategic and priority Managed Markets accounts. Position reports to Field Director /Senior Field Director /Executive Director . Essential Functions ... duties: Provides monthly reports on scientific leadership activities to Field Director including budget expenditures as directed Records all activities within One… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and statistical ... of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to Clinical Operations. Represents Clinical Development on Project Teams. Responsibilities Study Strategy: Provides the strategic direction to Biostats Data Mgmt & ... Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration with Translational Medicine/Clin… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder general supervision of an Executive Director /Senior Director , the Principal Scientist / Director is responsible for developing and ... support of their assigned projects. Position Description- The Principal Scientist / Director responsibilities include but are not limited to:Serve as a Regulatory… more
- Merck & Co. (Rahway, NJ)
- Job Description Director -QP2-IO We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology ... (QP2-IO) team in the role of Director . QP2-IO team is part of the Global Clinical...in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs), and representing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and/ or guide the QA review and approval of GLP and GCLP study protocols, clinical study reports, ICFs, external publications, and regulatory authority ... to design the audit framework globally for Research area, specifically GLP/GCLP studies .Partners with Audit and Compliance QA function to develop compliance and risk… more
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