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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
May 30
🏡 Remote – Anywhere in the UK
Learn about career opportunities, our culture, and our mission to improve human health.
Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
• Responsible for undertaking the technical activities required to build, test, maintain and archive clinical study databases throughout the duration of a study. • May act as the Lead Database Programmer • Create annotated (e) Case Report Forms (eCRF) • Build, test and maintain clinical databases • Program and test automated edit checks • Create and test files necessary for the electronic upload of data • Program and generate data listings for ongoing studies • Program and generate project tracking reports • Perform data transfers • Perform CR publishing requests • Manage database access • Archive electronic data and required documentation on study completion • Act as programming contact with sponsor to address database issues regarding or relating to area of expertise • Communicate the database set-up status and the achievement of milestones to internal or external project team members • May assist in the creation and documentation of new or revised departmental procedures
• A minimum of a college diploma/degree and 1-3 years of relevant experience. The ideal candidate will possess a background in computer science and database programming skills/experience.
• Home-based • Accommodations for job applicants with disabilities are available
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