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
Qualifications
College/University degree (Life Science, Pharmacy degree is a plus)
Demonstrated experience of managingclinical 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
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📌 Data Manager For Clinical Trials (Xico)
🏢 Psi Cro
📍 Xico