- Merck & Co. (Rahway, NJ)
- …clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications ;Developing clinical ... regarding safety and efficacy as well as new drug applications , clinical study reports, or publication;Participation in...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Rahway, NJ)
- …to support decisions regarding safety and efficacy as well as new drug applications , clinical study reports, or publication; andParticipation in internal and ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company… 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. (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)
- …- 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. (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
- 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. (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...will also be responsible for upskilling GCS in the applications used for reporting.- The Associate Director, BI&A will… more
- Merck & Co. (South San Francisco, CA)
- …DescriptionBrief Description of PositionTranslational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration ... with Immunology Discovery Sciences and late-stage Immunology Clinical Research. We work with all therapeutic areas within our Research Division with the role focused… more
- Merck & Co. (Chicago, IL)
- …with applicable policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the ... retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations (GCTO),Recommends study sites and identifies potential investigators… more
- Merck & Co. (Boston, MA)
- …(EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic community to positively impact Research and Development ... congressesLeads our Company's global scientific input forums to gain external scientific/ clinical insights in support of our Company's R&D strategySustains our… 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
- Novo Nordisk Inc. (Orlando, FL)
- …The EDCS must achieve sales goals by utilizing a patient-centric and clinical approach to engaging their customers and promoting Novo Nordisks portfolio of ... maintain advocacy of customers aligned to company, brand and clinical goals; the EDCS develops local strategies and executes...###. This contact is for accommodation requests only and cannot be used to inquire about the status of applications… more
- Formation Bio (New York, NY)
- …models for medical image analysis, focusing on MRI and X-ray modalities for clinical trial applications Design and implement automated image processing pipelines ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...drug development pipeline. In this role, you'll pioneer the application of computer vision and deep learning to medical… 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. (North Wales, PA)
- …management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions.This position involves… 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)
- …model-based strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within and across ... drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. Represent QP2 on...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… 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
