- Merck & Co. (Rahway, NJ)
- …Services SpecialistPRIMARY FUNCTIONPossess expertise in webcast pre-production, production, and post -production, which includes setup and operation of all video, ... all in-person and remote webcasts from pre-production, production, and post -productionProvide direction regarding scheduling and location staffing at a given… more
- Merck & Co. (Rahway, NJ)
- …accredited college/university with at least 12 years of relevant work experience post PhD defense.Required Experience and Skills: For BS/MS candidates, at least 15 ... years of relevant work experience post -graduation - OR - for PhD candidates with at...with at least 12 years of relevant work experience post PhD defense, where relevant work experience would include… more
- Merck & Co. (Rahway, NJ)
- …accredited college/university with at least 6 years of relevant work experience post PhD defense.Required Experience and Skills: -For BS/MS candidates, at least 11 ... years of relevant work experience post -graduation - OR - for PhD candidates with at...with at least 6 years of relevant work experience post PhD defense, where relevant work experience would include… more
- Merck & Co. (North Wales, PA)
- …health, or health economics strongly desired Required Experience and Skills: - 5+ years post PhD or 7+ years post master's degree of relevant experience in ... the areas of health economics, outcomes research, market access, HTA or related field. Demonstrated expertise in the design and implementation of clinical, epidemiological, or health economic studies Demonstrated expertise in the fields of outcomes research,… more
- Merck & Co. (Rahway, NJ)
- …leadership and laboratory capabilities in support of late-stage pipeline and post -market commercial manufacturing processes for vaccines and biologics. CCFS supports ... development activities, commercialization activities of late-stage pipeline and/ or post -market commercial manufacturing vaccines and biologics. For commercial programs,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of the US PED strategy into clinical development programs, post -authorization and commercial research activities and support/lead development, validation, and ... patient insights about disease and treatment to support clinical development, post -authorization, and commercial research activities across the lifecycle of drug… more
- Merck & Co. (Rahway, NJ)
- …and policy regarding IND/CTA, original NDA/MAA, agency background packages, post -approval submissions/variations, 510(K)s, CE markings. - Lead the development, ... of complex INDs, BLAs original NDA/MAA, agency background packages, post -approval submissions/variations, and replies to health authority questions according to… more
- Aequor (Seattle, WA)
- …biology, or a related discipline (or MS with relevant experience). Post -doctoral and/or analytical assay development experience is highly desirable, preferably ... biology, or a related discipline (or MS with relevant experience). Post -doctoral and/or analytical assay development experience is highly desirable, preferably… more
- Twist BioScience (South San Francisco, CA)
- …leverage new software features.Support Software UsersWork with teams to define post -release software issuesWork with internal software teams to resolve software ... record of successful software releases including validation, user training, post -release issue definition and resolution.Understanding of database design and SQL… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …planning and execution, data readiness, cutover planning and execution, and post -go-live supportAdvocate change management within CSPV department by assessing org ... FDA regulations supporting the submission of adverse events for post -marketing and investigative drugs. Understanding of global regulations preferredGood knowledge… more
- Merck & Co. (Rahway, NJ)
- …Oncology medicines span all phases of clinical development (pre-clinical to post -licensure). The Director will manage the entire cycle of clinical development, ... including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre-clinical and translational work for the purpose of generating early clinical development plan… more
- Merck & Co. (Rahway, NJ)
- …aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post -PCC to registration. Directors are leaders in the field of quantitative drug ... development, with a strong, integrated understanding of the strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative, cross-functional scientists to contribute… more
- Merck & Co. (Rahway, NJ)
- …aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post -PCC to registration. Associate Directors are emerging leaders in the field ... of quantitative drug development, with a developing understanding of the strategic elements of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams of… more
- Novo Nordisk Inc. (Irvine, CA)
- …and during company sponsored meetings: Strategic Planning- Pre-Call Planning, Post -Call Analysis Creates Customer Engagement-Open Purposefully, Uncover Needs Adapts ... Approach-Provide Solutions and Deliver Core Messages, Resolve Objections Call to Action-Gain Commitment with Impact, Transition For launch of new products, programs and services, establishes alignment among targeted physicians around the need for change, the… more
- Twist BioScience (South San Francisco, CA)
- …in Molecular Biology, Biochemistry, Chemistry or closely-related fields. Relevant post -doctoral or industrial experience is preferredStrong background in fundamental ... molecular biology techniques including DNA/RNA purification and quantification, PCR/qPCR, Molecular cloning, Enzymatic assays and Next Generation Sequencing (NGS).Experience in any one or more of the following: enzyme engineering, cell-free protein expression,… more
- Merck & Co. (Rahway, NJ)
- …and captures resulting actions, decisions, issues and responsible individuals.Leads post -meeting activities to ensure expected outcomes are achieved; follows up ... on action items appropriately with accountable staff.Coordinates and directs transformational and operational messages on behalf of GPAM leadership through various communications vehicles.Facilitates communication between our Research & Development Division… more
- Merck & Co. (Rahway, NJ)
- …process by preparing and reviewing consolidation journal entries, including post -closing adjustments for various business divisions and legal entities.Conduct ... comprehensive analyses of financial statement accounts, providing insightful commentary on absolute figures and variances to support the accuracy of the consolidated Income Statement and Balance Sheet, ensuring strict adherence to US GAAP.Develop and assemble… more
- Merck & Co. (Rahway, NJ)
- …oncology medicines span all phases of clinical development (pre-clinical to post -licensure). The Director will manage the entire cycle of clinical development, ... including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be responsible for: -Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and… more
- Merck & Co. (Rahway, NJ)
- …Our Oncology medicines span all phases of clinical development (pre-clinical to post -licensure). The Director will manage the entire cycle of clinical development, ... including study design, placement, monitoring, analysis, regulatory reporting, and publication. -- Specifically, the Director may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and… more
- Genmab (Plainsboro, NJ)
- …Pharmacology, Pharmacology, Pharmacokinetics, or related field with 15+ years of post -doctoral experience in relevant technical area10+ years of people/ functional ... management experience in relevant area, preferably in pharma/biotech industryBroad experience in therapeutic antibody R&D is required; experience in immune-oncology preferredWorking knowledge of Health Authority and Regulatory guidelines for drug… more
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