Your Responsibilities :
Oversee internal and external resources acting as lead programmer for complex software programs (using SAS and other technologies) that support monitoring, data management and data standards for across preclinical, clinical and epidemiological studies and the Data Repository and acts as a Subject Matter Expert.
This role ensures team deliverables are at the top of industry standards with respect to quality, performance and timelines.
Key responsabilities :
Basic qualifications :
Bachelors (minimum required) or Master Degree (preferred)
Engineering, Life Sciences, Computer Sciences, Mathematics and Physics or equivalent ( Ability to apply knowledge to manage complex processes and systems in the pharmaceutical industry)
Minimum 5 years Clinical Research or Information Systems or relevant scientific experience and demonstrated supervisory skills
Experience required to deliver assigned programs and projects in line with expectations in terms of time and cost and in compliance with DSCS processes .
Experience required to challenge and improve the operational processes within their area of expertise.
Language skills :
Preferred qualifications :
Why GSK? :
GSK is deeply committed to professional and personal development offering employment opportunities across a diverse collection of businesses and geographies.
So you’ll flourish in an inspiring environment where personal growth plays a vital part in the changing face of the business.
Most of all, you’ll enjoy the sense of purpose that comes from leading change in an industry that touches millions every day.
We offer :
Contact information :
You may apply for this position online by selecting the Apply now button.
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