- Merck & Co. (Rahway, NJ)
- …IndicatedValid Driving License:NoHazardous Material(s):N/ARequired Skills: Clinical Site Management, Clinical Testing, Data Analysis , Data Management, Data ... Description Responsibilities :This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders in Early… more
- Merck & Co. (Rahway, NJ)
- …clinical development, including study design, initiation, execution,- monitoring, analysis , regulatory reporting, publication, and presentation at national and ... are proud to be a company that embraces the value of bringing together, talented, and committed people with... Clinical Research Management, Clinical Testing, Clinical Trial Development, Data Analysis , Decision Making,… more
- Merck & Co. (Rahway, NJ)
- … to post-licensure). The Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis , regulatory ... are proud to be a company that embraces the value of bringing together, talented, and committed people with... Clinical Testing, Clinical Trial Planning, Clinical Trial Support, Cross-Functional Teamwork, Data Analysis ,… more
- Merck & Co. (North Wales, PA)
- …Study Design, Clinical Testing, Clinical Trial Compliance, Clinical Trial Management, Communication, Data Analysis , Dermatology, Drug Development, ... the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position,...are proud to be a company that embraces the value of bringing together, talented, and committed people with… more
- Merck & Co. (Rahway, NJ)
- … Study Design, Clinical Testing, Clinical Trial Compliance, Clinical Trial Management, Clinical Trials Analysis , Communication, Critical Thinking, ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this...are proud to be a company that embraces the value of bringing together, talented, and committed people with… 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 ... execution of statistical analysis and reporting deliverables (eg safety and efficacy ...listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post… more
- Merck & Co. (North Wales, PA)
- …contribute to the value evidence plan and associated studies which demonstrate clinical , economic, and patient-centered value . The work will support one or ... resources.To generate value evidence required by HTA/payers globally including value dossiers, evidence synthesis, clinical trial value endpoints,… more
- Novo Nordisk Inc. (Walnut Creek, CA)
- …Sales Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg, counterparts, ... and influence target physicians' approach to patient management and adds value by sharing new information and unique insights Leverages superior understanding… more
- Merck & Co. (North Wales, PA)
- …anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical trials, proposes solutions, and carries them out.3. ... investigators.9. Provides responses to queries relating to study design, analysis , and interpretation posed by the clinical ...are proud to be a company that embraces the value of bringing together, talented, and committed people with… more
- Merck & Co. (Rahway, NJ)
- … Databases, Clinical Site Management, Clinical Testing, Clinical Trials, Coaching, Communication, Computer Science, Data Analysis , Data Management, ... for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Overview - Basic Functions & Responsibility The Global Clinical Supply (GCS) organization is within our Research and Development division ... and is accountable for managing the 'end-to-end' integrated clinical supply chain across our Research & Development division portfolio to enable the execution of any… more
- Merck & Co. (Rahway, NJ)
- …review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release, and maintenance in support of ... our company's clinical supply programs. This person will also independently review...method validations, method transfers, analytical methods, specifications, certificates of analysis , etc.- Accountable for all assigned projects and communication… more
- Merck & Co. (Rahway, NJ)
- …or individual investigators.Provides responses to queries relating to study design, analysis , and interpretation posed by the clinical monitors, regulatory ... projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other company Research… more
- Merck & Co. (Rahway, NJ)
- …model-based strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across ... phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. Represent QP2 on cardiometabolic and… more
- Merck & Co. (Rahway, NJ)
- …teams to ensure patient access objectives and strategy are linked to clinical development, commercial and value evidence plans.Synthesize and communicate payer ... access to our medicines and vaccines at a price reflective of their value . We work collaboratively across the enterprise, and with regional and local market… more
- Merck & Co. (Rahway, NJ)
- …requirements for programming requests, retrieve required data, transform data into analysis /modeling datasets, and develop tables, listings and figures according to ... statistical/modeling analysis plan.Act as a key collaborator with statisticians, modelers,...field plus 3 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer… more
- Merck & Co. (North Wales, PA)
- …American Managed Care Pharmacy (AMCP) dossiers for US payers and Global Value Dossiers.Develops supplementary clinical data package in close partnership with ... Job DescriptionRole SummaryThe Principal Scientist/Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes… more
- Merck & Co. (Rahway, NJ)
- …high-quality products, test methods, and robust manufacturing processes for both clinical and commercial use. This position interacts extensively with subject-matter ... control and risk management techniques to positively support and influence clinical and commercial combination product development and launches. The incumbent must… more
- Merck & Co. (North Wales, PA)
- …decision-making skills, expertise in leading large teams in the development of novel clinical trial designs and analysis methods in oncology, experience in ... including regulatory submissionsDemonstrated history of development and execution of innovative clinical trial designs and exploration of novel analysis methods… more
- Merck & Co. (South San Francisco, CA)
- …ms of experienced sci e ntis ts to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You ... model-based strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across… more