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Sr. Statistical programmer

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Full Remote
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Offer summary

Qualifications:

Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, or Life Sciences., 6 - 8 years of experience in SAS programming with a focus on complex data analysis projects., Proficiency in BASE SAS, SAS/STAT, SAS/MACRO, and SAS/GRAPH., Strong background in statistical analysis and familiarity with clinical trial data and CDISC standards..

Key responsabilities:

  • Develop, validate, and execute SAS programs for data extraction and statistical analysis.
  • Generate tables, listings, and figures to summarize analytical results and conduct statistical modeling.
  • Collaborate with cross-functional teams and communicate project requirements effectively.
  • Provide mentorship to junior programmers and ensure data integrity through quality checks.

Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
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Job description

Responsibilities:
  • Develop, validate, and execute SAS programs for data extraction, transformation, and statistical analysis.
  • Perform complex data manipulations, including merging, sorting, and aggregating large datasets.
  • Generate tables, listings, and figures (TLFs) to summarize and present analytical results.
  • Conduct statistical modelling and hypothesis testing as required.
  • Ensure the accuracy and consistency of data by conducting quality checks and validating analysis results.
  • Follow best practices for programming and maintain a well-documented codebase.
  • Review and QC programs and outputs generated by junior programmers.
  • Collaborate with cross-functional teams, including statisticians, data scientists, clinical researchers, and project managers.
  • Communicate effectively with team members and stakeholders to understand project requirements and deliverables.
  • Stay up-to-date with industry standards and regulatory guidelines (e.g., FDA, ICH) to ensure data integrity and compliance.
  • Contribute to the preparation of regulatory submissions by providing statistical outputs and documentation.
  • Manage multiple projects simultaneously, ensuring timelines and deliverables are met.
  • Provide mentorship and guidance to junior SAS programmers as needed.
  • Prepare and maintain documentation, including analysis plans, data dictionaries, and programming specifications.
  • Assist in the development of standard operating procedures (SOPs) related to SAS programming.

Requirements:

  • Bachelor's or Master's degree in a relevant field (e.g., Statistics, Computer Science, Mathematics & Life Sciencess).
  • 6 - 8 years of experience in SAS programming, with a proven track record of working on complex data analysis projects.
  • Pharma/biotech/medical device/CRO experience.
  • Proficiency in SAS programming, including BASE SAS, SAS/STAT, SAS/MACRO, and SAS/GRAPH.
  • strong background in statistical analysis and data management.
  • Familiarity with clinical trial data and CDISC standards is often preferred.
  • Strong problem-solving skills and attention to detail.
  • Excellent communication and interpersonal skills.
  • Ability to work both independently and collaboratively within a team.

Required profile

Experience

Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Quality Assurance
  • Communication
  • Teamwork
  • Detail Oriented
  • Social Skills
  • Problem Solving

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