Manager, Statistical Programming Consultant

ClinChoice

About The Position

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds... ClinChoice is currently recruiting for a Manager, Statistical Programming Consultant to join our client’s team —an exciting opportunity to lead impactful statistical strategy in a dynamic environment. Role Overview 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. 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. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

Requirements

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.

Responsibilities

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.
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.
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.