Associate Director Statistical Programmer

Job Title: Associate Director, Statistical Programmer
Company: Biopharma
Location: Boston, MA

Brio Resource Group is a Life Sciences Executive Search Firm committed to providing rare talent on an exclusive search basis to the Biopharma, Pharma, Device, and CRO industries. We work on behalf of organizations that value true talent acquisition partners and specialize in supporting emerging Biopharma companies offering life-changing therapies. Our many years of experience, subject matter expertise, comprehensive search process, and genuine passion to deliver rare talent defines Brio.

Position Overview:
We’ve partnered with an innovative biopharma company that’s looking to hire a Associate Director of Statistical Programming. In this role, you will be responsible for providing hands-on programming support and technical guidance for the development of SAS programs, as well as overseeing CRO programming deliverables. You will work closely with internal and external teams to ensure accurate, timely statistical programming deliverables in support of regulatory submissions and reporting.

Opportunity Highlights:

  • Lead statistical programming activities and oversee CRO deliverables, ensuring compliance with CDISC standards for SDTM and ADaM

  • Perform hands-on SAS programming to generate TLFs and support ad hoc requests

  • Review data management documents and support internal data management teams

  • Manage production, validation, and review of tables, listings, and figures for clinical study reports and regulatory submissions

  • Develop and maintain statistical programming standards, processes, and SOPs

  • Collaborate with cross-functional teams to ensure project timelines and goals are met

Position Requirements:

  • Master’s degree in Statistics, Mathematics, Computer Science, or a related field

  • 10+ years of experience as a statistical programmer in the biopharma, pharmaceutical, or CRO industry

  • Experience with NDA submissions is a plus

  • Proficiency in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, and SAS/ODS

  • Knowledge of industry standards including ICH guidelines, CDISC standards, and FDA guidelines

  • CNS drug development experience a plus

  • Ability to manage multiple projects in a fast-paced environment

  • Excellent communication skills and the ability to collaborate effectively with internal and external teams

  • Results-oriented, highly motivated, and flexible in problem-solving

We welcome the opportunity to provide a full job description upon resume review.