Your responsibilities will include Analysis of project data (e.g. trial data) and data processing Statistical programming, development of reusable programs (e.g. functions, macros), data visualization, program validation, output generation Support non-clinical / clinical development in all phases, study planning (protocol,
Your responsibilities will include Hands on data processing and analysis of project data (e.g. trial data, biomarkers, gene expression data) Develop predictive models, identify subgroups, perform cutoff determination using basic / advanced statistical methods Statistical programming, development
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Country Approval Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Site Contract Specialist – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact
Your responsibilities will include Analysis of project data (e.g. trial data) and data processing Statistical programming with SAS and/or R, development of reusable programs (e.g. macros), data visualization, and output generation Specification and creation of (CDISC) analysis datasets
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than