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| Job Location | Histon |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
CK Group are recruiting for a RAVE Subject Matter Expert, to join a small but growing Data Management team - not just to deliver data management for this exciting portfolio of studies, but to help shape and influence how a Pharmaceutical Company drives data management excellence for the future. This role can be site or home based with occasional visits to the site in Cambridge on a permanent basis. RAVE SME Role: Principal responsibilities will include to:- Be responsible and accountable for planning, organisation, leadership and coordination of all data management activities on assigned projects (Phase I to IV) right from the database set-up to project closure with minimum supervision.- Work closely with Data Management vendors to ensure quality and timely data management deliverables.- Utilise your Medidata Rave knowledge (including RAVE screen build and edit check programming).- Be the RAVE EDC subject matter expert supporting DM colleagues and assigned CROs.- Spend approximately 50% of your time as the Data Management Study Lead and 50% in the RAVE SME role. Your Background:- Bachelors or Masters Degree in Life Sciences.- Demonstrate sound knowledge of Drug Development Process and Clinical Data Management processes.- Extensive experience in Clinical Data Management in the pharmaceutical industry.- Strong experience of Medidata Rave eCRF screen build and edit check programming (SME level).- Good Knowledge of ICH and GCP guidelines.- Experience leading projects from study start-up to database lock.Full job description available upon request.Apply:For more information or to apply for this RAVE SME position, please contact Stephanie Maccioni on or email , quoting job ref 48404.It is essential that applicants hold entitlement to work in the UK.CLINGEN