Data Manager for Clinical Trials

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. Please submit your CV in English Responsibilities will include: Track database set-up, testing, maintenance and data entry Communicate with clients, project teams and vendors on data management matters Review study documents, design and develop project specific guidelines and instructions Design eCRF, Data Management and Data Validation Plans and test EDC databases Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation Code medical data Track and report metrics leading to database lock Coordinate the processing, dispatch and archiving of CRFs/queries Maintain Clinical Data Management working files Perform database QC checks, prepare and attend audits Train site staff and project teams on CRF completion and data management topics College/University degree (Life Science, Pharmacy degree is a plus) Demonstrated experience of managing clinical or medical data Full working proficiency in English Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) Proficiency in MS Office applications Organisational and time management skills Ability to work independently and multi-task 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.