- Merck & Co. (Rahway, NJ)
- …limited to Investigational New Drugs, Investigational Medicinal Product Dossier s, and Clinical Trial Application s.Ability to work closely with cross-functional ... with superior product quality and allow speedy progression for clinical studies and commercial launch. The candidate will be...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (North Wales, PA)
- …SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position, you will have the ... cross functional team.Job ResponsibilitiesResponsible for leading specific aspects of clinical /scientific execution of clinical protocol(s). This may… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Insmed Incorporated (San Diego, CA)
- …and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director of Clinical Quality Assurance ... GCPs, acts as quality lead on the gene therapy clinical development team, and collaborates on other related activities...To request reasonable accommodation to participate in the job application or interview process, please contact us by email… more
- Merck & Co. (Rahway, NJ)
- …- This position leads the scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this position, you will have the ... team . - Job Responsibilities - Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s) . This may include: Serving as… 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 c ... ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… 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 ... Research & Development Division portfolio of clinical trials. -GCS is accountable for the planning, sourcing,...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… 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's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience.The AVP will also be responsible… more
- Eisai, Inc (Nutley, NJ)
- …development.Provide technical guidance to the programming team in terms of application design, development, validationGood understanding in Clinical Data ... is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
- Aequor (Pearl River, LA)
- …in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities ... the world. ROLE SUMMARY We are seeking a highly motivated full-stack web application developer (contract) with exceptional programming skills to join Vaccines R&D in… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... : 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. (Rahway, NJ)
- …listings, and graphics required for clinical trial decision-making, regulatory requests, clinical study reports, and new drug application filing. Produce SAS ... the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other programming colleagues and biostatisticians and/or… more
- Merck & Co. (South San Francisco, CA)
- …of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist with a proven ... 5-year experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as Dermatology,… more
- Merck & Co. (Rahway, NJ)
- …quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. ... and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be… more
- Merck & Co. (South San Francisco, CA)
- …strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development. The successful candidate will have an essential strategic ... strategies and interact with various stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role… more
- Merck & Co. (Rahway, NJ)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (North Wales, PA)
- …the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your ... management, communication, and collaboration skills in support of our clinical trials.Job ResponsibilitiesResponsible for the operational planning, feasibility, execution… more
