- Merck & Co. (North Wales, PA)
- …determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and ... clinical trials for investigational drugs.Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as… more
- Merck & Co. (Upper Gwynedd, PA)
- …determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and ... clinical trials for investigational drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …role in guiding toxicology strategy from early research through IND-enabling studies and into clinical development, ensuring regulatory compliance and scientific ... cell and gene therapy.Design, implement, and interpret nonclinical safety studies , including IND-enabling toxicology, biodistribution, and pharmacokinetics.Provide scientific and… more
- Merck & Co. (North Wales, PA)
- …internal teams and external partners, design non-interventional and data synthesis studies , author study protocols, develop measurement questionnaires, case ... report forms, data analysis plans, final study reports, scientific presentations, and publications.Responsible for study -related contracting, budgets, and… more
- Merck & Co. (North Wales, PA)
- …biostatistics in early or late clinical development planning to ensure that study designs are consistent with program objectives and meet worldwide regulatory and ... and interprets results from clinical trials to meet objectives of the study protocol.- Independently applies and implements basic and complex statistical techniques… more
- Eisai, Inc (Pittsburgh, PA)
- …Maintain and demonstrate thorough and up-to-date knowledge of disease state, study methodology, clinical information, and product data.Demonstrate full knowledge of ... Research Support Facilitate review and follow up of submitted Investigator-Initiated Studies (IISs) and assist with Eisai sponsored trials.Serve as primary contact… more
- Merck & Co. (North Wales, PA)
- …Skills:Broad knowledge and experience in epidemiologic research and observational study designHands-on research experience using real-world data or other large-scale ... Process, Mathematical Biology, Molecular Biology, Multidisciplinary Collaboration, Multi-Management, Observational Studies , Oncology, Parasitology, Programming Languages, Project Reviews, Public Health,… more
- Merck & Co. (North Wales, PA)
- …will be a key collaborator with BARDS epidemiologists and partner with study teams to effectively implement RWE standards to execute project plans efficiently. ... Submissions, Epidemiology, Innovation, Machine Learning (ML), Numerical Analysis, Observational Studies , Pharmaceutical Development, REMOTE_SKILL-1-52891, Software Development, Stakeholder Relationship Management,… more
- Merck & Co. (North Wales, PA)
- …Management, Business Technology, Change Management, Clinical Data Management, Clinical Study Management, Clinical Study Protocols, Clinical Trials, ... Communication, Data Analysis, Data Governance, Data Processing, Data Validation, Decision Making, Ethical Standards, Good Clinical Practice (GCP), Life Science, Microsoft Azure {+ 3 more}Preferred Skills: Current Employees apply HERE Current Contingent Workers… more
- Merck & Co. (North Wales, PA)
- …safety and efficacy analysis datasets, tables, listings, figures) for early oncology studies . The incumbent is responsible for the design and maintenance of ... statistical datasets that support multiple stakeholder groups which include clinical development, and safety evaluation. The position is a key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently… more
