This page tracks remote scientist openings that are location-eligible for Texas.
Open jobs
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$75,000 - $140,799
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9 Jobs
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• Direct the planning, preparation, writing and review of portions of aggregate reports • Organize and direct liaison for activities with affiliates and other internal Amgen partners regarding products • Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO • Review and provide input and support on study protocols, statistical analysis plans and other clinical study-related documents • Review of AEs/SAEs from clinical trials as needed • Review standard design of tables, figures, and listings for safety data from clinical studies • Participate in development of safety-related data collection forms for clinical studies • Participate in study team meetings as requested or needed • Perform data analysis to evaluate safety signals and write up analysis results • Search and review adverse event data, literature, and other safety-relevant data for the purpose of signal detection • Prepare presentation of the Global Safety Team’s recommendations on safety issues to the cross-functional decision-making body • Assist GSO in the development of risk management strategy and activities: Provides contents for risk management plans • Develop or update strategy and content for regional risk management plans • Assist GSOs to oversee risk minimization activities including tracking of activities as needed. • Evaluate risk minimization activity • Prepare response to regulatory inquiries related to risk management plans under the guidance of GSO • Support activities related to new drug applications and other regulatory filings • Assist GSO in developing a strategy for safety-related regulatory activities • Provide safety contents for filings • Undertake activities delegated by the QPPV as detailed in the PV System Master File and maintain a state of inspection readiness • Be representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility
• Provide scientific and technical support for health-related research, programs, and initiatives • Analyze and interpret scientific data • Support research and program activities • Prepare technical documentation • Collaborate with project teams and stakeholders to meet program objectives
• Provides scientific and technical support for health-related research, programs, and initiatives • Analyzes and interprets scientific data, supporting research and program activities • Prepares technical documentation, and collaborates with project teams and stakeholders to meet program objectives while ensuring compliance with applicable federal requirements
We are a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.
• RWE and Bioinformatics Analysis: Lead large-scale genomics data analysis, specifically in Chronic Kidney Disease (CKD), to extract actionable insights. • Predictive Analytics & Modeling: Develop and implement robust predictive models to forecast clinical trends and outcomes using RWE and genomics data. • Data Visualization and Communication: Create and implement innovative data visualization strategies to effectively communicate complex genomic analysis results. • Project Leadership: Own and manage genomics projects from initial concept through to final delivery, ensuring all initiatives are completed efficiently (on time and within budget). • Cross-Functional Partnership: Collaborate closely with Sales, R&D, Data Science, Business Development, Medical Affairs, and Engineering. • Data Stewardship: Facilitate the integration of genomics data with diverse data types to enrich analyses. • Reporting and Publication: Prepare detailed reports and manuscripts for publication. • Innovation and Development: Maintain current knowledge of the latest developments in genomics and bioinformatics and propose new methods for analysis.
Creating the Power of the Stars on Earth
• Provide theoretical and simulation support on the beam smoothing project. • Coordinate laser beam requirements, including picket and drive beam design and beam port design. • Support the roadmap, partnering with the diagnostics team and leading physics efforts. • Provide theoretical support for implementation in the DUED code. • Provide theoretical support for LPI science across LPI experiments and simulations. • Partner closely with the beam smoothing team, the laser and science teams working on beam requirements, the target design team, and the target physics team on LPI risk mitigation and imprint/hydrodynamic instabilities.
• Contribute to ongoing research using Lagrangian modeling to understand sources and sinks of trace gases and other air pollutants, through independent completion of both externally and self-directed research tasks • Expand existing research interests and capabilities beyond this initial project's immediate goals • Regularly develop innovative techniques to apply existing satellite and model datasets, or create new observational datasets, to answer scientific questions • Show adaptability in performing research tasks outside their immediate research area as needed with minimal spin-up time • Develop their own externally funded research program through research grant proposals and contracts with non-profit and industry clients
At Cytovale, we’re focused on more rapid and insightful ways to diagnose fast-moving and immune-mediated diseases.
• Serve as a primary technical resource during the pre-sales process • Present IntelliSep technology and its clinical value confidently to laboratory stakeholders • Deliver engaging presentations and live instrument demonstrations • Develop strong relationships with laboratory leaders and key stakeholders • Address customer questions and concerns related to implementation and operational impact • Support customer implementations from project kickoff through go-live and post-implementation support • Deliver comprehensive and structured operator training • Troubleshoot and resolve technical, workflow, and operational issues • Provide ongoing consultation and support to maximize customer success
• Support a Centers for Disease Control and Prevention (CDC) public health evaluation initiative • Conduct public health evaluation activities through evaluation planning, implementation, data analysis, technical assistance and reporting • Develop large-scale program logic models • Facilitate internal and external partner meetings • Provide assistance or training on evaluation methods, concepts, and tools • Conduct implementation research including assessing fidelity and contextual factors
• Support public health evaluation activities through evaluation planning, implementation, data analysis, technical assistance and reporting • Conduct systematic assessment of CDC public health evaluation initiatives • Develop program logic models and facilitate internal and external partner meetings • Provide assistance or training on evaluation methods, concepts, and tools
Python, SQL
