Testing of data entry screens and the preparation of relevant testing documentation.
Perform Data Entry of the Case Report Forms
Reconciliation of 1st Pass and 2nd Pass Data Entry
Annotated CRF for defining standards as per CDISC/CDASH as per system requirements
Initial review Case Report Form data to check whether CRF are incomplete, inaccurate, and inconsistent identify and resolved data discrepancies.
Discrepancy Data Management (Generation of DCF, Printing DCF, Resolving queries
Perform or assist in all aspects of DM process as related to processing QC /review/ UAT and subsequent updations of the findings of the data.
Clean data for study close out and perform all database lock procedures
To assist manager in holding QA audits and providing Corrective and Preventive action plan
Solve operational problems related with database (front end) and Clinical Data Management processes.
Archiving and maintain study documentation in individual study files in accordance with all applicable SOPs.
Experience 0- 1 years
Age 22 – 27 Years
Industry Type Pharmaceutical
Functional Area Clinical Data Management
Education B.Sc./Diploma in IT
Compensation At par with the Industry
Department Clinical Research
Location New Delhi
Contact Panacea Biotec Ltd
Email corporate@panaceabiotec.com, rohitkumar1@panaceabiotec.com
Website http://www.panaceabiotec.com/
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