Statistical Programmer II

October 2

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Clinical Outcomes Solutions

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Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics

51 - 200

Description

• Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. • As a Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. • This is an exciting time to be a part of this new program. • As a Statistical Programmer, you will leverage your advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials.

Requirements

• At least 3+ years of relevant experience in statistical programming in the clinical development environment • BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject • Excellent SAS data manipulation, analysis and reporting skills • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners • Excellent oral and written English communication skills • Ability to provide quality output and deliverables, in adherence with challenging timelines • Willingness and ability to learn and follow Company’s standard processes and procedures. • Ability to effectively perform complex statistical programming and related tasks • Willingness and ability to provide guidance to team members on technical and process questions