Biostatistical Programming Manager
On-siteLondon, England, United Kingdom or Cambridge, England, United Kingdom
Job Summary
Develop, test, and QC SAS, R, and SQL programs for large healthcare datasets while overseeing study implementation and quality control. Lead and mentor a team of programmers to ensure accurate, timely deliverables, managing project priorities, resources, workflows, and timelines with key stakeholders. Develop and review programming plans, dataset specifications, macros, functions, and utilities to ensure analyses are accurate, complete, and compliant with policies and SOPs. Represent programming in cross-functional meetings, support audits, controlled-document development, and contribute to study documentation including SAPs, CRFs, and Data Management Plans. Drive innovation, efficiency, and organizational growth within the Center for Observational Research.
Required Qualifications
- Degree educated in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific subject
- Demonstrated experience in the pharmaceutical industry and within a regulated environment
- Extensive SAS or R programming experience for complex data manipulation and analysis
- Proven experience with database programming using SQL
- Experience with real world healthcare data such as the Clinical Practice Research Datalink (CPRD), German Disease Analyzer, MarketScan, Optum, DRG, PharMetrics, Medicare or other Electronic Medical Records (EMR) databases
- Vendor relationship management or related experience with functional service providers
- Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model as well as with Databricks or other high performance computing environment
- Experience with UNIX operating system
- Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace
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