SAS EG Jobs

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SAS EG
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πŸ“ UK, EU

🧭 Contract

πŸ” Clinical development, Pharmaceutical, Biotechnology

🏒 Company: ClinChoice

  • MS or PhD in Statistics, Biostatistics or related field.
  • Strong SAS skills are required.
  • Experience required in Respiratory & Immunology TA (Asthma Study).
  • Strong oral and written communication skills.
  • Demonstrated understanding of statistics, drug development process, and relevant FDA regulations.
  • Experience with clinical trials and interaction with Regulatory Agencies, especially FDA.

  • Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
  • Provide statistical oversight and assure quality and consistency with project requirements.
  • Ensure data for statistical analyses are complete, accurate, and consistent.
  • Manage statistical analysis plans and the accuracy and timeliness of statistical input into reports.
  • Demonstrate understanding of statistical concepts, correct flaws in reasoning and interpretation.
  • Mentor peers in statistical methodology and train less experienced statisticians.

LeadershipData AnalysisSAS EGData analysisCommunication SkillsAnalytical SkillsCollaborationMicrosoft ExcelMentoring

Posted 2024-11-09
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πŸ“ United States

🧭 Contract

πŸ” Clinical research and development

🏒 Company: ClinChoice

  • MS or PhD in Statistics, Biostatistics or related field; PhD with 2-4 years or MS with 5-7 years of experience.
  • Strong SAS skills.
  • Experience in interpreting data for clinical purposes.
  • Respiratory & Immunology therapeutic area experience.
  • Strong oral and written communication skills.
  • Pharmaceutical, CRO, or related industry experience with clinical trials.

  • Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
  • Provide statistical oversight and ensure data quality and consistency.
  • Verify the accuracy and timeliness of statistical input into reports.
  • Demonstrate understanding of statistical concepts and mentor peers.
  • Manage assignments and coordinate activities of statisticians across projects.

LeadershipSAS EGCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaborationMentoring

Posted 2024-11-09
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πŸ“ US, Canada

🧭 Full-Time

πŸ” Biotechnology/Pharmaceuticals

🏒 Company: Precision Medicine Group

  • Master's degree or equivalent in Statistics, Biostatistics, or related field with 10+ years experience, or PhD with 7+ years experience.
  • Experience with SAS.
  • Knowledge of ICH guidelines, CDISC data structures, and FDA guidelines.
  • Advanced statistical concepts understanding.
  • Preferred experience with Oncology and rare diseases, late phase submissions, and consulting on study design.

  • Generate and verify randomization schedules.
  • Develop and review statistical methods of clinical study protocols.
  • Provide and verify sample size calculations and perform advanced calculations.
  • Author and review statistical analysis plans.
  • Generate analysis datasets, tables, figures, and listings using SAS.
  • Conduct quality control for statistical SAS programs and documents.
  • Serve as a consultant to global staff with regional understanding.
  • Provide statistical analysis for Data Monitoring Committees.
  • Interact with sponsors, project managers, and vendors.
  • Lead statistical activities, perform budget health reviews, and oversee projects.

LeadershipProject ManagementData AnalysisSAS EGProject CoordinationCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-11-09
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πŸ“ US, Canada

🧭 Full-Time

πŸ’Έ 133000 - 180000 USD per year

πŸ” Pharmaceutical/Biotech

🏒 Company: Precision for Medicine

  • Master's degree or equivalent in Statistics, Biostatistics, or related field with 10+ years of experience.
  • PhD degree in Statistics, Biostatistics, or related field with 7+ years of experience.
  • Experience with SAS.
  • Knowledge of ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.
  • Advanced statistical concepts and techniques.
  • Preferred experience with Oncology and rare diseases.
  • Broad experience with late phase and/or submissions.
  • Experience consulting on study design.

  • Generate and/or verify randomization schedules.
  • Develop and review statistical methods for clinical study protocols including complex study designs.
  • Provide and/or verify sample size calculations and perform advanced calculations like adaptive design.
  • Author and review statistical analysis plans, including table, figure, and listing shells.
  • Generate analysis datasets, tables, figures, and listings using SAS.
  • Perform quality control for SAS programs and other study documents.
  • Serve as a biostatistical consultant internally and externally.
  • Provide statistical analysis and reports to Data Monitoring Committees.
  • Work with sponsors and project managers on statistics-related project components.
  • Lead all statistical activities for study within timelines.

LeadershipProject ManagementData AnalysisProduct ManagementSAS EGProject CoordinationCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-11-09
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πŸ“ United States

🧭 Regular Full-Time

πŸ’Έ 84000 - 117000 USD per year

πŸ” Healthcare economics and outcomes research

🏒 Company: Precision AQ

  • 3-5 years of experience in real-world evidence (RWE).
  • Master’s degree in health services research (e.g., health economics, public policy, epidemiology).
  • Proficiency in SAS or R.
  • Ability to work effectively as part of a diverse team.
  • Awareness of financial performance on projects.

  • Contribute to multiple projects with cross-functional staff.
  • Serve as the analytics expert on projects.
  • Design real-world evidence studies.
  • Develop study protocols and analysis plans.
  • Perform analyses of primary and secondary data.
  • Communicate study results to stakeholders.

LeadershipData AnalysisSAS EGCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-07
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πŸ“ North Carolina, United States

🧭 Full-Time

πŸ’Έ 114730 - 173000 USD per year

πŸ” Biopharmaceutical industry

🏒 Company: Verista

  • Bachelor's Degree in sciences or engineering required; advanced degrees preferred.
  • 10+ years of industry relevant experience.
  • Demonstrated experience with R&D Clinical applications, such as Statistical Analysis software and clinical data analysis tools.
  • Proficient understanding of R&D clinical processes in the biopharmaceutical industry.
  • Outstanding verbal and written communication skills.
  • Strong understanding of regulatory frameworks.
  • Ability to work independently and adapt to changes.

  • Responsible for the implementation and support of technology and informatics systems and programs.
  • Support development, implementation, operation, and continuous improvement of Laboratory Operations, Clinical, Biostatistics and Data Management, Bioprocess R&D and Regulatory/Risk Management applications.
  • Report to the IT Director, R&D Systems.
  • Work with SAS Office Analytics, Electronic Trial Master File (eTMF), AWS, Electronic Lab Notebook (ELN), and other digital tools.

AWSLeadershipProject ManagementAgileBusiness AnalysisData AnalysisPeople ManagementProduct ManagementSAS EGSCRUMProject CoordinationCross-functional Team LeadershipAmazon Web ServicesData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAgile methodologiesAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communicationMultitasking

Posted 2024-11-07
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πŸ“ Canada

🧭 Contract

πŸ” Clinical Trials, Hematology

🏒 Company: ClinChoice

  • Bachelor’s degree in computer science, statistics, or related scientific disciplines with 8 years of clinical programming experience.
  • Master’s degree in CS, statistics, or related disciplines with 7 years of clinical programming experience.
  • Oncology/Hematology therapeutic area experience required.
  • ISS & ISE experience is required.
  • Working knowledge of ICH and Good Clinical Practices.
  • Strong communication and coordination skills.

  • Lead and support all programming activities per project strategies.
  • Develop Tables, Figures, Listings (TFLs) deliverables from SAS programs.
  • Customize outputs and graphics based on delivery specifications.
  • Support the programming deliveries of clinical studies.
  • Communicate and escalate risks associated with assigned studies.

LeadershipData AnalysisSAS EGData analysisCommunication SkillsAnalytical SkillsMicrosoft Excel

Posted 2024-11-07
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πŸ“ United States

🧭 Regular Full-Time

πŸ’Έ 84000 - 117000 USD per year

πŸ” Health Economics and Outcomes Research

🏒 Company: Precision Medicine Group

  • 3-5 years of experience in Real World Evidence (RWE).
  • Master’s degree in a subject related to health services research, such as health economics, public policy, epidemiology, biostatistics, or public health.
  • Proficiency in SAS or R.
  • Ability to work effectively both individually and as part of a diverse team.
  • Awareness of financial performance on projects.

  • Contribute to multiple projects as an analytics expert on cross-functional teams.
  • Design RWE studies and develop study protocols.
  • Perform analyses of primary and secondary data.
  • Communicate study results internally and externally.

LeadershipSQLData AnalysisNumpySAS EGCross-functional Team LeadershipData analysisCommunication SkillsAnalytical SkillsCollaborationProblem SolvingAttention to detailOrganizational skillsPresentation skillsTime ManagementWritten communication

Posted 2024-11-07
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πŸ“ Poland, United Kingdom, Canada, South Africa

🧭 Full-Time

πŸ” Life Sciences

🏒 Company: Quanticate

  • Extensive knowledge of statistical software packages, particularly SAS.
  • Extensive knowledge of SQL.
  • Qualified to degree level or equivalent, preferably in a numerate discipline.
  • PC skills.
  • Good organizational skills.
  • Strong communication skills (oral and written).
  • Good analytical skills and attention to detail.

  • Program tables, figures, listings, and derived datasets as per request.
  • Perform quality control checks and complete related documentation.
  • Follow Project Management procedures.
  • Communicate effectively with the OR team.
  • Provide input for process improvements.
  • Support training and development of junior programmers.

Project ManagementSQLData AnalysisSAS EGData analysisCommunication SkillsAnalytical SkillsOrganizational skills

Posted 2024-10-26
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πŸ“ Canada, United Kingdom, Poland, South Africa

🧭 Full-Time

πŸ” Life Sciences

🏒 Company: Quanticate

  • Good knowledge of statistical software packages (particularly SAS).
  • Good knowledge of SQL.
  • Qualified to degree level or equivalent, preferably in a numerate discipline.
  • Should have PC skills.
  • Good organisational skills, communication skills (oral and written).
  • Good analytical skills and attention to detail.

  • Program tables, figures and listings and derived datasets according to the request description.
  • Perform quality control checks and complete quality control documentation for programming plans, specifications, outputs/derived datasets.
  • Perform other reasonable programming tasks as requested by management.
  • Follow appropriate Project Management procedures.
  • Communicate effectively with OR team.
  • Provide input to improvements to processes, procedures and standards.
  • Support the training and development of other programmers.

Project ManagementSQLData AnalysisSAS EGData analysisCommunication SkillsAnalytical SkillsAttention to detail

Posted 2024-10-26
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