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PAREXEL International Corporation Job Title
Senior Statistical Programmer - FSP, UK

Company
PAREXEL International Corporation

Job Description
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Parexel.com
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We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it
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Senior Statistical Programmer - FSP, UK
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Job ID
79511BR
Sheffield, England, United Kingdom
The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Senior Statistical Programmer can fill the Statistical Programming Lead role on projects, and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas as required. Further, the Senior Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.
Qualifications
Proficiency in SAS
Proven Lead Statistical Programming experience within related environment (minimum 6 years experience)
Knowledge of the programming and reporting process
Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application
Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement
Demonstrate ability to learn new systems and function in an evolving technical environment
Strong leadership ability.
Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently
Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change
Attention to detail.
Excellent analytical skills.
Good presentation skills.
Tenacity to work in an innovative environment.
Ability to negotiate and influence in order to achieve results.
Business/Operational skills that include customer focus, commitment to quality management and problem solving.
Good business awareness/business development skills (including financial awareness).
Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
Work effectively in a quality-focused environment.
Demonstrate commitment to refine quality processes.
Effective time management in order to meet daily metrics or team objectives
Show commitment to and perform consistently high quality work
Education
Educated to degree level in a relevant discipline and/or equivalent work experience
Language Skills
Competent in written and oral English.
Excellent communication skills.
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