Associate Director Statistical Programming

Website Lenox Executive Search

Full Time
Location: Cambridge, MA (Hybrid Remote potential) On-Site is preferred due to level of responsibility.

No direct reports: Opportunity to grow the group and oversee as projects are brought back in-house.
Salary is commensurate with experience.

Reports to: Sr. Director, Clinical Data Sciences.

Qualifications:
 Utilized SAS to generate output used for data modeling, clinical trial reports and regulatory
submission packages (i.e., tables, listing, figures, as well as SDTM, SEND, and ADaM datasets)
within the pharmaceutical industry.
 Experience in the oncology therapeutic space is a plus. A solid understanding of the CDISC SDTM
and ADaM IGs is required.
 Write SAS programs to generate tables, listings, and figures.
 Lead programming activities for assigned projects.
 Provide technical leadership with regard to programming standards and validation procedures.
 Build SEND, SDTM and ADaM datasets from clinical databases following CDISC guidelines.
 Create mapping specifications for derived datasets.
 Develop SAS macros, templates and utilities for data cleaning and reporting.
 Implement analyses specified in Statistical Analysis Plans.
 Utilize SAS to fit statistical models (i.e., PROC REG, PROC IML and PROC GLM).
 Validate SAS programs used to create output in a regulated environment.
 Work in tandem with Biostatisticians and Data Managers on various clinical projects.

Education/Experience:
 Bachelor or Masters’ level degree in statistics/biostatistics, mathematics, computer science or
engineering
 9+ years of pharmaceutical/biotechnology/CRO experience

*Position is eligible for bonus, option awards and benefits including medical, dental and life insurance,
401(k) participation, paid vacation and paid holidays. Successful candidate must be authorized to
work in the United States.

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