Job Description
• Develop Case Report Form (CRF), electronic and/or paper.
• Performing Data entry for paper CRF.
• Participate in the review of Clinical research documents (eg. Protocols, Case Report Forms, Reports)
• Participates in EDC database (DB) specification process
• Execution of test scripts and maintaining logs for User Acceptance Testing (UAT)
• Reconcile electronic data transfers from vendor to Sponsor.
• Provide Clinical data management support to Clinical Operations team and Biostatistics Team
• Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design.
• Develop Data Management Plan (DMP), maintains DMP throughout Lifecycle of study project and ensure DMP is followed according to study Design and requirements.
• Provides input and reviews clinical trial database design including User Acceptance Testing (UAT).
• Lead EDC database (DB) specification process.
• Reconcile electronic data transfers from vendor to Sponsor.
• Perform training on data management software and practices or trial specific topics as required.
Requirements
Qualification-Bpharm/Mpharm/any life sciences background.
Only male candidates required.
Experience- candidates who have done 3months to 6 months course in Data management required.
The candidate should speak English and Hindi well.
Candidates residing in Hyderabad only reply.
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