A global provider of clinical research services in the UK is seeking a Lead Programmer to serve as a Centralized Monitoring Analyst. The role involves managing the Centralized Monitoring process, requiring strong SAS programming skills and experience in pharmaceutical research. Key responsibilities include supporting the Centralized Monitoring Lead, programming quality assessments, and maintaining platform specifications. The ideal candidate will have at least 3 years of relevant experience and demonstrated communication and organizational skills. Visa sponsorship is not available for this position.
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