Statistical Programmer II

September 30

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Act as an internal Subject Matter Expert and work independently to support various programming activities related to analysis and reporting of clinical study data. • Perform as Statistical Programming Coordinator on projects and interact with Sponsors, Data Operation Lead and other functions as a key contact with regard to statistical programming issues. • Use efficient programming techniques to produce and QC of derived datasets and TLF. • Create/modify standard macros and applications to improve efficiency. • Develop wider knowledge of SAS and other relevant programming languages and processes. • Understanding regulatory requirements concerning industry technical standards, maintain supporting documentation in accordance with WSOPs/guidelines. • Provide relevant training and mentorship to staff and project teams.

Requirements

• Knowledge of WSOPs/ICH-GCP and System Life Cycle methodologies. • Excellent communication (written & oral) skills and strong leadership ability. • Strong organizational skills, flexible to change and team work. • Ability to manage complex projects and business operational skills. • Study lead experience. • For Associate Manager and Manager Role you must have people management (LM) experience. • First degree (undergraduate or equivalent) in a relevant discipline is preferred or equivalent. • Competent in written English. • Good communication skills.