Roles & Responsibilities
• Responsible for clinical writing
• Interact with client matters related to changes and information required
• Review blinded data tables for CSR writing
• Address customer comments at each draft stage
• Review of documentation prior to release
• Compliance to customer templates and ICH Guidelines, as applicable
• Implement and validate QC findings as appropriate, in compliance with NC
Handling Procedure
• Compliance to Document Control Procedure
• Compliance to Record Control Procedure
Job Requirements
• Post-Graduate in scientific discipline, preferably pharmaceutical or any other life science.
• 1+ years experience in technical or medical writing desirable (not compulsory)
• Excellent scientific writing skills
• Ability to understand clinical data
• Proficiency with MS Office applications
• Good communication skills
• Familiarity with ISO 9001:2008 requirements
Click here for more info and to apply
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