[Hiring] Manager, Statistical Programming Consultant @ClinChoice

Role Description

We are seeking an experienced and motivated Manager, Statistical Programming to lead programming activities within the Biometrics group. This role will oversee clinical programming deliverables, drive quality and compliance, support regulatory submissions, and mentor a team of programmers. The ideal candidate will have strong expertise in SAS (and/or R), deep knowledge of CDISC standards, experience with oncology clinical trials, and excellent leadership skills.

Key Responsibilities:

• Leadership & Strategy
  • Lead and mentor a team of statistical programmers, fostering development and high performance.
  • Oversee internal and vendor/CRO programming deliverables, ensuring timelines and quality expectations are met.
  • Establish and maintain programming standards, documentation, and best practices.
  • Support planning, resourcing, and prioritization for programming activities across multiple studies.
• Programming & Technical Delivery
  • Oversee development and validation of SDTM and ADaM datasets according to CDISC standards and oncology study requirements.
  • Supervise creation of Tables, Listings, and Figures (TLFs) for clinical study reporting and regulatory submissions.
  • Ensure all deliverables are of high quality, reproducible, and aligned with regulatory expectations (e.g., FDA, EMA).
  • Support automation and efficiency initiatives using SAS and/or R.
  • Perform and review QC checks, resolving programming and data issues.
• Cross-Functional Collaboration
  • Partner closely with Biostatistics, Clinical Data Management, Medical Writing, and Regulatory teams.
  • Participate in study team meetings, contributing programming perspective to clinical and data discussions.
  • Support preparation of submission-ready deliverables, including reviewer guides, traceability documents, and regulatory artifacts.

Qualifications

• Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related field.
• 9–11+ years of statistical programming experience in the pharmaceutical/biotech/CRO environment.
• Strong proficiency in SAS programming; experience with R is a plus.
• Expert understanding of CDISC standards (SDTM, ADaM).
• Experience managing or mentoring programming teams.
• Demonstrated experience supporting regulatory submissions.
• Excellent communication skills and ability to work collaboratively across functions.

Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Company Description

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.