Lead Data Manager for Clinical Trials.

hace 5 días

Buenos Aires, Argentina PSI A tiempo completo

Job Description The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects.   Communication Primary communication point for project teams and company departments with regard to clinical data management Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting  Data Management Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables.  Primary responsibility for clinical data management activities within clinical projects, including, but not limited to:Study documents reviewData Management plan and other project-specific guidelines and instructions development and reviewCo-ordinate/perform user acceptance testingDevelopment of Data Validation Plan/Edit Check SpecificationsData entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issuesData validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of dataNon-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues)Database edits (paper CRF studies)Manual CRF review (non-medical checks)Clinical database lockCoordination and supervision of processing, dispatch and archiving of CRFs/queries Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol Development of CRF completion guidelines Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required) SAE reconciliation Electronic data transfer (import/export) specifications review and approval Document Management Liaison with Document Center with regard to maintenance of TMF and eTMF Quality Control Database QC checks performance and documentation Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management Training Training of Assistant Data Managers Project-specific training of investigators and clinical team in CRF completion Corporate/Departmental Assignments Investigator Meetings preparation/attendance Meetings and teleconferences organized by client/vendor preparation/attendance Qualifications College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities At least 3 years of experience of full scope of data management responsibilities in international EDC studies At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable) Project data management experience is a plus Full working proficiency in English Organizational and managerial skills Additional Information Advance your career in clinical research and develop new skillsets whilst growing with the organization.

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