Descrizione:
Experteer OverviewIn this role you will manage clinical data processes to ensure high-quality, timely trials. You will work within PSI’s global clinical operations to handle data management tasks across studies, collaborating with clients, project teams and vendors. You will design and validate data collection and reporting plans, oversee data entry and reconciliation, and support QA and audits. You will play a key part in driving data integrity and efficiency, using leading CDMS tools to enable database lock. This is a chance to contribute to impactful clinical research within a respected, inclusive CRO.Retribuzione / BenefitsTrack database set-up, testing, maintenance and data entryCommunicate with clients, project teams and vendors on data management mattersReview study documents, design and develop project specific guidelines and instructionsDesign eCRF, Data Management and Data Validation Plans and test EDC databasesEnsure data entry, follow-up and validation, including manual CRF review and SAE reconciliationCode medical dataTrack and report metrics leading to database lockCoordinate the processing, dispatch and archiving of CRFs/queriesMaintain Clinical Data Management working filesPerform database QC checks, prepare and attend auditsTrain site staff and project teams on CRF completion and data management topicsResponsabilitàCollege/University degree (Life Science, Pharmacy degree is a plus)Demonstrated experience of managing clinical or medical dataFull working proficiency in EnglishExperience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)Proficiency in MS Office applicationsOrganisational and time management skillsAbility to work independently and multi-taskRequisiti fondamentalibase salary 34,000–52,000 gross annual salarybonusincentive plansother benefits may apply #J-18808-Ljbffr