- Merck & Co. (Rahway, NJ)
- …to customers.Perform statistical analysis to support biological and vaccine clinical assays.Author and review detailed statistical reports suitable for submission ... people from diverse backgrounds and expertise, including research scientists, clinical scientists, regulatory experts, IT specialists, etc.Identify opportunities to… more
- Merck & Co. (North Wales, PA)
- …or marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development ( pre - clinical to post-licensure). The Director will ... including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Evaluating pre - clinical and translational work for the purpose of… more
- Merck & Co. (Rahway, NJ)
- …marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development ( pre - clinical to post-licensure). The Senior Director ... reporting, and publication.Specifically, the Senior Director may be responsible for:Evaluating pre - clinical and translational work for the purpose of generating… more
- Merck & Co. (Rahway, NJ)
- …regulatory reporting, and publication.Specifically, the position may be responsible for:Evaluating pre - clinical and translational work for the purpose of ... with a cross-functional group of experts in commercialization, regulatory affairs, statistics , and manufacturing to manage clinical development projects; and… more
- Merck & Co. (North Wales, PA)
- …opinion leaders.Specifically, the Associate Vice President may be responsible for:Evaluating pre - clinical and translational work for the purpose of generating ... with a cross-functional group of experts in commercialization, regulatory affairs, statistics , and manufacturing to manage clinical development projects; and… more
- Merck & Co. (North Wales, PA)
- …or related field and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science, Statistics , Applied Mathematics, Life ... This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more… more
- Merck & Co. (North Wales, PA)
- …and support for related drug/vaccine projects in Late Development Statistics .Interacts with Clinical , Regulatory, Statistical Programming, Data Management, ... human health. Education and Minimum Requirement: PhD or equivalent degree in statistics /biostatistics or related discipline with a minimum of 3 years relevant work… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics , Applied Mathematics, Life ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
- Merck & Co. (North Wales, PA)
- …within an Asset team. Our Company's Oncology medicines span all phases of clinical development ( pre - clinical to post-licensure). The Director will manage ... value inflection points.--Identifying, negotiating and maintaining critical external partnerships.--Evaluating pre - clinical and translational work for the purpose… more
- Merck & Co. (Rahway, NJ)
- …cross-functional teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for cardiac, respiratory, metabolic, ... Develop model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and… more
- Merck & Co. (North Wales, PA)
- …Skills Education and Minimum Requirement :BA/BS in Computer Science, Statistics , Applied Mathematics, Information Technology, Life Sciences, Engineering, or related ... field plus 9 years in a clinical trial environment (Analysis & Reporting,- Information Technology, Data Management etc.) in the pharmaceutical industry, and 3 years… more
- Merck & Co. (Rahway, NJ)
- …in the role of Associate Director. The team is part of the Global Clinical Development organization and has oversight over drug development 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… more
- Merck & Co. (North Wales, PA)
- …Preferred skills : - Understanding of the principles of clinical research, clinical trial design , fundamental statistics , and safety data reporting- - ... Plain Language Summaries (PLS), including the Protocol PLS and Results PLS, of clinical studies per our company's process es and standards to ensure compliance with… more
- Merck & Co. (Rahway, NJ)
- …team in the role of Director. QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development 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… more
- Merck & Co. (Rahway, NJ)
- …pharmacometrics capabilities like comparator modeling, model-based meta-analysis (MBMA) and clinical trial simulations (CTS) into programs and thereby strengthening ... quantitative approaches that seek to improve cycle time, cost/size, number of trials, clinical trial design and Go/No Go decisionsServe as a subject matter expert… more
- Merck & Co. (Rahway, NJ)
- …Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications.Ability to design, execute and/or direct the ... and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development.A… more
- Merck & Co. (Boston, MA)
- …that accelerate the decision-making process from hit identification to clinical candidate delivery across different therapeutic areas and modalities at ... conjugates, and targeted protein degraders.Initiate and apply novel ML, statistics , and cheminformatics techniques to improve hit identification and hit-to-lead… more
- Merck & Co. (Rahway, NJ)
- …Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specificationsAbility to design, execute and/or direct the ... and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process developmentA strong… more
- Merck (Upper Gwynedd, PA)
- …to customers. + Perform statistical analysis to support biological and vaccine clinical assays. + Author and review detailed statistical reports suitable for ... people from diverse backgrounds and expertise, including research scientists, clinical scientists, regulatory experts, IT specialists, etc. + Identify opportunities… more
- San Jose State University (San Jose, CA)
- … Advisor Apply now (https://secure.dc4.pageuppeople.com/apply/873/gateway/default.aspx?c=apply&lJobID=534345&lJobSourceTypeID=837&sLanguage=en-us) Job no: 534345 ... Director of International Recruitment and Partnerships, the International Recruitment Advisor provides admission information, academic support and advising to… more
