Essential job duties:

¨(20%) Data Planning – responsible for all data aspects of studies including review of draft protocols,attendingClinicStartUpMeetings,supportingthe workbook(CRF) designprocess, training plans for non-standard study data capture and attend Biometrics start up meetings as required.

¨(20%)EnsurethatthedataentryandQC ofdoseescalationdataiscompletedwithinthe required timelines.

¨(15%)CompletedailyongoingQCofallstudydataacrossClinicalOperations includingdaily shop floor QC.

¨(15%)ActasprinciplehostforsponsorCRFmonitoringvisits.Promotingaprofessionalimage of Leeds CRU and building strong collaborative working relationships with CRA’s.

¨(10%) QueryResolution– ensureall databasequeries; sponsors written data queries, CRA monitoringqueriesandinternalQAaudit findings areresolvedwithintheagreedtimelines.

¨(10%) Responsible forensuringtheweeklyData EntrySchedule is updatedandaccurately reflects study workload.

¨(5%) StudyCloseDown-Ensure completedCRF’saresignedbythe Principal or Associate Investigator and that all CRF’s and source data is archived on completion of the study.

¨(5%)Performotherjobrelateddutiesas assigned.

Minimum requirements

Typicallylookingfor1-2yearsofdata handlingexperience.Experiencecanbefroma clinical or non-clinical background. For example financial data handlingbackground.

¨Excellentwrittenandoralcommunicationskills

¨Abilitytoprioritizeworkloads

¨Goodorganizationalskills

¨Previouscustomerserviceexperiencedesirable