We interpreted Newtown, PA as Newtown, PA. Other options include:
Newtown (Schuylkill County), PA
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Clinical Project Scientist…
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Kelly Services
(Horsham, PA)
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** Clinical Project Scientist ** Hybrid - Onsite in Horsham, PA Monday - Wednesday (Thursday & Friday Remote) **Job Summary:** This individual contributor will
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Team and support one to two therapeutic areas. The Clinical Project Scientist is responsible...Committee tracker) + Assist with user acceptable testing for clinical trial systems + Prepare presentations and…
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Kelly Services (01/28/25)
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Senior Clinical Scientist , Early…
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Bristol Myers Squibb
(Princeton, NJ)
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…more: careers.bms.com/working-with-us . **Functional Area Description** The Early Development Clinical Scientist function provides scientific expertise necessary
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Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. + Successfully leads, plans, and executes …
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Bristol Myers Squibb (02/02/25)
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Principal Scientist , CMC Regulatory…
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J&J Family of Companies
(Spring House, PA)
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…technical oversight for the generation of the CMC dossier for marketing and clinical trial submissions. Coordinates the timelines, virtual document, and Quality
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Johnson & Johnson is recruiting for a Principal Scientist , CMC Regulatory Dossier Development which can be...of regulatory documents, including CMC sections for marketing and clinical trial submissions is preferred. + Experience…
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J&J Family of Companies (02/09/25)
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Associate Principal Scientist , Statistical…
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Merck
(North Wales, PA)
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…Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics,
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position is a key collaborator with statistics and other project stakeholders in ensuring that project plans...7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and…
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Merck (12/13/24)
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Scientist , Statistical Programming- Hybrid
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Merck
(Upper Gwynedd, PA)
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…programmers have a key role in the analysis and reporting of our company's clinical trial databases. The statistical programmer uses their analytical skills to
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about our company's products. + Attend training in key software languages and clinical trial processes required to conduct statistical analysis and reporting. +…
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Merck (02/11/25)
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Senior Principal Scientist , Bioanalysis (1…
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J&J Family of Companies
(Spring House, PA)
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…programs and represent the bioanalytical function to cross-functional team members including Clinical Pharmacology and Pharmacometrics, Clinical Trial Leads,
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Johnson and Johnson is currently seeking a Senior Principal Scientist , Bioanalysis located in Spring House, PA or Beerse, Belgium. At Johnson & Johnson, we believe…
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J&J Family of Companies (02/07/25)
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Senior Scientist , Statistical Programming
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Merck
(North Wales, PA)
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…3 years of experience with all of the following: SAS programming in a clinical trial environment; developing analysis and reporting deliverables for Research and
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potential medical breakthroughs. + Review quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality…
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Merck (02/13/25)
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Sr. Scientist , Statistical Programming-…
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Merck
(North Wales, PA)
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…of experience is with all of the following: SAS programming in a clinical trial environment including data steps, procedures, SAS/MACRO, and SAS/GRAPH;
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medical breakthroughs. + Support statistical programming activities for Early Oncology clinical development projects. + Review the quality and reliability of …
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Merck (02/07/25)
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Associate Director, Clinical Sciences…
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J&J Family of Companies
(Spring House, PA)
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…tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/. The Clinical Project Scientist (CPS) works in the Oncology
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Scientists. The position reports to a more senior Clinical Project Scientist . Essential Functions:...participate in or lead aspects of, medical review of clinical trial data, including adverse events, efficacy…
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J&J Family of Companies (02/11/25)
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Senior Director -Safety Surveillance
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Novo Nordisk
(Plainsboro, NJ)
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…(phase I trials) + Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure (IB),
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publications + Provide proactive safety communication by participation in project / trial groups/teams established, as appropriate and conducts Investigator…
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Novo Nordisk (02/13/25)
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Associate Director, Biostatistics
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Bristol Myers Squibb
(Princeton, NJ)
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…leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,
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a core member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, preparation…
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Bristol Myers Squibb (02/12/25)
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