Novartis
Scientific Writer II Life-science Degree
or equivalent B.Sc./, M.Sc./M.Pharma
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.
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
TO APPLY CLICK HERE
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