Principal Statistical Programmer

Recruiter
PAREXEL
Location
Bedfordshire
Posted
19 Jan 2018
Closes
18 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
The Principal Statistical Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors, and works independently to support various programing activities related to the analysis and reporting of clinical study data. In addition, the Principal Statistical Programmer can fill the Primary Statistical Programmer role on projects and liaise with sponsors, Data Operations Leads, and other functional areas as required. Furthermore, the Principal Statistical Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets.• Excellent analytical skills.• Proficiency in SAS.• Extensive knowledge and understanding of the programming and reporting process.• Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.• Ability to learn new systems and function in an evolving technical environment.• Strong project management skills.• Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.• Attention to detail.• Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently.• Work effectively in a quality-focused environment.• Effective time management in order to meet daily metrics or team objectives.• Show commitment to and perform consistently high quality work.• Strong organizational skills, ability to manage competing priorities, and flexibility to change.• Business/operational skills that include customer focus, commitment to quality management, and problem solving.• Demonstrate commitment to refine quality processes.• Good presentation skills.• 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.QualificationsProficiency in SAS• Knowledge of the programming and reporting process• Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any otherapplicable local and international regulations such as 21 CFR Part 11 and proven practicalapplication• Demonstrated application of CRS concepts to achieve best practice and promote continuousimprovement• 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 asrequired) as well as independently• Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible tochange• 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 andproblem 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 workEducation• Educated to degree level in a relevant discipline and/or equivalent work experienceLanguage Skills• Competent in written and oral English.• Excellent communication skills.

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