Principal SAS Programmer

Veristat International, Ltd; England; Remote; GBP 60,000 - 90,000; Full time

Job summary

A leading clinical research organization is seeking a Principal SAS Programmer to lead programming activities for CSRs and analyses. The ideal candidate will have extensive SAS programming experience with clinical trial data and a degree in a related field. Responsibilities include supporting SDTM and ADaM activities and leading a team of programmers to deliver high-quality results. Strong communication and leadership skills are essential for this role.

Qualifications

• Minimum 10 years of SAS programming experience with clinical trial data (Bachelor's degree).
• Minimum 8 years of SAS programming experience with clinical trial data (Master's degree).
• Good knowledge of CDISC SDTM and ADaM Implementation Guidelines.

Responsibilities

• Lead programming activities for CSRs, DSMBs, and analyses.
• Support migration activities for SDTM and ADaM.
• Coordinate and lead a team of programmers.

Skills

SAS programming

Regulatory requirements knowledge

Excellent communication skills

Organizational skills

Leadership skills

Education

Bachelor's or Master's Degree in relevant field

Job description

The Principal SAS Programmer independently leads the programming activities for various purposes including CSRs, DSMBs, interim analyses, manuscripts, etc. Mainly supports statistical programming of statistical analysis plan (SAP)-planned tables, data listings, and graphs for CSRs, as well as integrated summaries of safety and efficacy, ad hoc analyses and electronic submission deliverables, such as datasets, data documentation, programs, programming table of contents, and patient profiles.

In addition, the Principal SAS Programmer supports migration activities in the creation of Standard Data Tabulation Model (SDTM) and production of the Analysis Data Model (ADaM). The Principal SAS Programmer is also responsible for monitoring and meeting assigned program milestones, and will coordinate and lead a team of programmers to accomplish tasks.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams

• Bachelor’s Degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 10 years of SAS programming experience with clinical trial data OR Master’s Degree in in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 8 years of SAS programming experience with clinical trial data.

• Good working knowledge of CDISC SDTM and ADaM Implementation Guidelines.

• Excellent knowledge of regulatory requirements and drug development process.

• Excellent organizational skills and verbal/written communication skills.

• Ability to work independently as well as lead programming teams.

• Strong communication skill set with peers, business partners, and Sponsors.

• Leadership skills to lead project team to deliver high quality deliverables on time and working directly with the Sponsor to meet the project delivery expectations.

• Must be fluent in English (written and verbal).

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

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Equal Opportunity Employer

Veristat is proud to provide exceptional services to our clients, assisting in the successful development of innovations that improve and save lives. We are equally proud to recruit, develop and retain the best and the brightest talent across a variety of business functions to make that happen. We are an Equal Opportunity Employer that values the strength and creativity that diversity brings to our workplace.