SAS EG Jobs

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SAS EG

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🔥 Statistical SAS Programmer (m/f/d)

Posted about 23 hours ago

📍 Bulgaria

🔍 Technology

🏢 Company: Tieto_Careers_External_Site

Bachelor’s/master's degree in engineering, Computer Science, or equivalent experience.
At least 3-5 years of experience as a SAS developer.
Experience with SAS DI Studio, SAS Base, and SAS EG is a significant advantage.
Minimum of 4+ years of experience in software engineering with SDLC tools and languages like Oracle.
At least 2+ years of experience with Red Hat Linux or UNIX.
Proven experience working with Teradata.
Well-versed with SAS Base and SAS macros in a Linux/UNIX environment.
Thorough experience with relational databases.
A minimum of 3+ years of experience with version control systems like GitHub, SVN, TFVC, or TFSGit.
Familiarity with analytics and prior experience in the financial services industry is a bonus.
Excellent spoken and written English and strong communication skills.

Understand and carry out software engineering processes for designing, developing, documenting, reviewing, testing, analyzing, and releasing codes.
Write high-quality codes that are easy to test using modern abstractions and frameworks.
Manage complex tasks using problem-solving skills and analytical abilities.
Work with various team members including product managers, UI/UX designers, developers, and marketing managers.
Collaborate with technical authors to build specifications and contribute to operational documentation.
Identify and implement modifications to existing systems.
Resolve integration and incompatibility issues in existing applications.

Git Oracle SAS EG

Posted about 23 hours ago

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🔥 SAS Programing Team Lead (m/f/d)

Posted about 23 hours ago

📍 Bulgaria

🔍 Technology

🏢 Company: Tieto_Careers_External_Site

Bachelor’s or Master’s degree in Engineering, Computer Science, or a related field (or equivalent experience).
Proven experience in building and managing teams.
Demonstrated ability to mentor and develop junior team members.
Experience as a SAS programmer.
Experience with SAS DI Studio, SAS Base, SAS EG is a big advantage.
Extensive experience working with relational databases.
Proficiency in version control systems such as GitHub, SVN, TFVC, or TFSGit.
Familiarity with analytics and related tools is a plus.
Hands-on experience in application production and support.
Prior experience in the financial services industry will be an advantage.
Excellent spoken and written English.
Strong communication skills.

Recruit, interview, and build the SAS programming team.
Lead and manage the Statistical Programming Team, ensuring alignment with project goals and timelines.
Provide technical support and mentorship to junior programmers to foster professional growth.
Maintain a strong focus on client satisfaction through exceptional service delivery.
Design, develop, and maintain SAS programs to support data analysis and reporting.
Conduct high-quality statistical analyses and generate detailed reports.
Collaborate with cross-functional teams to ensure data accuracy and integrity.
Ensure all processes and outputs comply with regulatory requirements and company standards.
Participate in continuous improvement initiatives by reviewing and optimizing existing SAS code and workflows.

Data Analysis Git SAS EG

Posted about 23 hours ago

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🔥 Lead/Principal Statistical Programmer Consultant(Hematology/Oncology-Clinical Trials) REMOTE

Posted 11 days ago

📍 United States

🧭 Contract

🔍 Clinical development, pharmaceutical, biotechnology, medical device, consumer health

🏢 Company: ClinChoice

Bachelor’s degree in computer science, statistics, or related scientific disciplines with 6 years of clinical programming (CDISC) experience; Master’s degree with 8 years of experience.
Oncology/Hematology TA experience is required.
Experience with ISS & ISE is required.
Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial process, and related regulatory requirements.
Good understanding of the clinical drug development process.
Strong communication and coordination skills.
Current knowledge of technical and regulatory requirements for the role.
Ability to manage concurrent activities proactively.

Lead and support all programming activities per project strategies.
Develop Tables, Figures, Listings (TFLs) deliverables from existing SAS programs and from scratch for new outputs.
Customize outputs and graphics according to delivery specifications.
Support Programming deliveries of clinical studies.
Program independently with high efficiency and quality.
Contribute to best practices for quality and efficiency.
Ensure compliance with standards and usage of automation.
Plan and support team activities and tasks.
Communicate and escalate risks within assigned studies.

SAS EG

Posted 11 days ago

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🔥 Research Scientist - Real World Evidence

Posted 2 months ago

📍 United States

🧭 Regular Full-Time

💸 84000 - 117000 USD per year

🔍 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.

Leadership Data Analysis SAS EG Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration Problem Solving Attention to detail Organizational skills Presentation skills Time Management Written communication

Posted 2 months ago

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🔥 Lead/Principal Statistical Programmer Consultant(Hematology, Clinical Trials) REMOTE@CANADA

Posted 2 months ago

📍 Canada

🧭 Contract

🔍 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.

Leadership Data Analysis SAS EG Communication Skills Analytical Skills Microsoft Excel

Posted 2 months ago

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🔥 Research Scientist - Real World Evidence

Posted 2 months ago

📍 United States

🧭 Regular Full-Time

💸 84000 - 117000 USD per year

🔍 Health Economics and Outcomes Research

🏢 Company: Precision Medicine Group👥 1001-5000💰 $35,160,000 almost 4 years agoPharmaceutical Biotechnology Medical Precision Medicine Health Care

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.

Leadership SQL Data Analysis Numpy SAS EG Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration Problem Solving Attention to detail Organizational skills Presentation skills Time Management Written communication

Posted 2 months ago

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🔥 Associate Director / Director, Statistical Programming

Posted 3 months ago

📍 Cambridge, MA

🧭 Full-Time

🔍 Pharmaceuticals / Oncology

🏢 Company: Nuvalent, Inc.

Master’s Degree in statistics, mathematics, computer science, or a related scientific/medical field.
8+ years of SAS statistical programming experience in clinical trials.
Advanced SAS programming skills, including Macro language and reporting.
Knowledge of CDISC SDTM and ADaM model standards.
Familiarity with regulatory guidelines related to clinical trials.
Experience with outsourcing programming activities and CRO management.
Advanced understanding of statistical concepts.

Function as lead programmer to produce and/or validate tables, listings, figures, and analysis datasets.
Write specifications for programming needs.
Develop/review TFL shells, SDTM and ADaM specifications.
Ensure the accuracy of final databases, analyses, and reports.
Partner with or oversee CROs for programming tasks.
Manage project timelines and schedules.
Identify problems and enhance efficiency through global tools.

Leadership Project Management People Management SAS EG Project Coordination Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration

Posted 3 months ago

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🔥 Principal Statistician

Posted 3 months ago

📍 United Kingdom

🧭 Full-Time

🔍 Pharmaceutical, biotechnology, medical devices

🏢 Company: Quanticate👥 251-500 Pharmaceutical Biotechnology Professional Networking Health Care

MSc in Biostatistics, Statistics or equivalent.
Strong statistical expertise with experience in clinical trials.
Experience in SAS programming.
Extensive knowledge of regulatory requirements for clinical trials.
Strong project management and leadership skills with experience leading large-scale projects.
Excellent verbal and written communication skills.
Ability to work independently and as part of a team.
Willingness to travel when needed.

Serve as lead statistician for clinical trials including planning, analysing, and reporting, ensuring that all deliverables are met on time and to a high level of quality.
Develop and validate statistical models and analyses based on study protocols.
Write statistical analysis plans and reports.
Provide guidance and mentorship to other statisticians in the group.
Collaborate with cross-functional teams to develop study protocols and ensure they meet regulatory requirements.
To potentially take line management responsibility for junior statisticians within the team.
To lead statistical consultancy projects as required, providing expert statistical advice on all statistical aspects of study design and conduct.
Perform ad hoc statistical duties as required.

Leadership Project Management Data Analysis SAS EG Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration

Posted 3 months ago

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🔥 Junior Research Associate, JRA

Posted 4 months ago

📍 Philippines, Mexico

🧭 Full-Time

🔍 Market Research

🏢 Company: Hireframe👥 101-250 Management Consulting Consulting Sales Professional Services

Some prior market research experience, preferably with a research vendor company
Knowledge of research techniques through coursework, internships, or work experience
Familiarity with market research tools and statistical software (such as SPSS, SAS, Qualtrics, and/or Alchemer)
Proficiency in Excel, PowerPoint, and Outlook
Strong attention to detail, ability to prioritize tasks, and contribute to multiple projects simultaneously
Capable of working independently and within teams
Excellent interpersonal, problem-solving, and project management skills
Excellent verbal and written communication skills

Perform tasks and responsibilities required with thoroughness to produce high-quality, high-accuracy market research deliverables.
Load, test, and proofread all research surveys and content on staging before posting live to production.
Assure data accuracy and relevance to objectives at every step in the project process to ensure the data is both internally consistent and demonstrates face validity.
Design and program research instruments (utilizing multiple methodologies, both qualitative and quantitative within the community) to answer research and business questions.
Prioritize tasks, communicate effectively, and remain flexible to meet client needs.
Ensure all project components are executed within the scope contract and/or project proposal, and all timelines for met.
Assist with daily moderation of research activities in the communities and extract insights. Oversee data collection and ensure quotas are met and data quality is achieved.

Leadership Project Management Data Analysis SAS EG Project Coordination Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration Microsoft Excel PowerPoint

Posted 4 months ago

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🔥 Senior/Principal Biostatistician

Posted 5 months ago

📍 Poland, Hungary, Serbia, Romania, Slovakia

🔍 Clinical Research

Master's degree / PhD in Statistics, Biostatistics, or equivalent.
At least 7 to 10 years experience as a Biostatistician in a Clinical Research Organization.
Extensive knowledge of industry standards like ICH guidelines and FDA guidelines.
Experience with SAS programming.
Familiarity with complex statistical methods applicable to Phase I-IV clinical trials.

Generate randomization schedules.
Assist with statistical methods review of clinical study protocols.
Provide and verify sample size calculations.
Develop and author statistical analysis plans.
Validate analysis datasets and conduct quality control for statistical SAS programs.
Provide statistical support for regulatory agency analyses and ad-hoc requests.
Train and mentor new biostatisticians.
Interact directly with sponsors and project managers.

Leadership Data Analysis People Management SAS EG Communication Skills Analytical Skills Collaboration C (Programming language)

Posted 5 months ago

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