DATA MANAGER FOR CLINICAL TRIALS

<p>Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.</p><p><u><strong>Please submit your CV in English</strong></u></p><p><strong>Responsibilities will include:</strong></p><ul><li>Track database set-up, testing, maintenance and data entry</li><li>Communicate with clients, project teams and vendors on data management matters</li><li>Review study documents, design and develop project specific guidelines and instructions</li><li>Design eCRF, Data Management and Data Validation Plans and test EDC databases</li><li>Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation</li><li>Code medical data</li><li>Track and report metrics leading to database lock</li><li>Coordinate the processing, dispatch and archiving of CRFs/queries</li><li>Maintain Clinical Data Management working files</li><li>Perform database QC checks, prepare and attend audits</li><li>Train site staff and project teams on CRF completion and data management topics</li></ul> <ul><li>College/University degree (Life Science, Pharmacy degree is a plus)</li><li>Demonstrated experience of managing&#xa0;clinical or medical data</li><li>Full working proficiency in English</li><li>Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)</li><li>Proficiency in MS Office applications</li><li>Organisational and time management skills</li><li>Ability to work independently and multi-task</li></ul> <p>If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.&#xa0;</p>