Novartis
Scientific Writer II Life-science degree
or equivalent B.Sc./equivalent with 4 years Clinical Research (CR) experience,
M.Sc./M.Pharma
- Job Description
- Your responsibilities include, but are not limited to:
- • Prepares literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles etc..
- • Performs quality control (QC) checking / proof reading of above documents to meet customer expectation.
- • Manages assigned individual projects. Obtains feedback from customers.
- • Complies with and support group’s project management tool, standards, policies and initiatives.
- • Follows Novartis specifications for documentation, specifically Novstyle, templates etc.
- • Follows and track clinical trial milestones for assigned projects.
- • Maintains records for all assigned projects including archiving.
- • Maintains audit, SOP and training compliance. Performs additional tasks as assigned.
Minimum requirements
• Life-science degree or
equivalent B.Sc./equivalent with 4 years Clinical Research (CR) experience,
M.Sc./M.Pharma + 2 years of CR experience.
• Desired – Doctoral
degree, Qualification in Med Good written and oral English skills in Medical
Sciences (MBBS/MD/equivalent) PhD + 1 year of CR experience, MBBS/equivalent +
1 year of CR experience
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