Job Details

A company is looking for an Associate Director, Statistical Programming.Key ResponsibilitiesOversee and manage CROs, ensuring quality and adherence to timelines and budgetsValidate datasets and prepare submission-readiness datasets for BLA filingConduct hands-on statistical programming for various analyses and collaborate with internal teamsRequired QualificationsBS (10+ years) or MS (8+ years) in Statistics, Life Sciences, Computer Science, or related fieldsExperience in statistical programming within the pharmaceutical industryStrong SAS programming skills and familiarity with RExperience managing CROs and knowledge of drug development regulationsUnderstanding of clinical trial design and regulatory reporting requirements