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Statistical Programming Opportunities at Parexel

As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and therapeutic areas, or choose to focus your career on working with a specific sponsor and gaining in depth knowledge of a specific therapeutic area and compound.

Senior Statistical Programmer (Russia)

Job ID 60727BR Moscow, Moscow, Russia
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Coordinator role on projects, and liaise with sponsors, Data Operations Leads, and other functional areas as required. •Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to.
•Lead a statistical programming team to successful completion of a study within given timelines and budget
•Monitor project resourcing, project budgets, and identify changes in scope
•Interact with Sponsors as the key contact with regard to statistical programming issues
•Provide technical support and advice to the internal team
•Check own work in an ongoing way to ensure first-time quality
•Ensure quality control (QC) on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance with corporate quality standards, WSOPs/Guidelines, ICH-GCP and/or other international regulatory requirements are performed.

Qualifications

• Educated to a degree level (biological science, pharmacy or other health related discipline preferred) or relevant clinical or business equivalent
•5 plus years proficiency in SAS programming
•2+ years of ADaM, CDISC or SDTM
•Lead experience in Pharma
•Attention to detail, ability to be self-driven and solid organization skills
•Excellent communication skills (verbal and written)

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