Medical
Writer II @ Novartis
Minimum
requirements
•
M.Pharm/M.Sc Good communication skills in english (written, verbal,
presentations) 2 to 3 years of regulatory medical writing experience or other
relevant pharma industry experience combined with scientific and regulatory
knowledge, plus in-depth knowledge of medical writing processes.
•
Good operational knowledge of clinical trial reporting. Good knowledge of
biostatistics principles.
•
Strong ability to prioritize and manage multiple demands and projects.
Knowledge of and experience in global regulatory environment and processes (key
regulatory bodies, key documents, approval processes, safety reporting
requirements).
•
Good experience in managing global, cross functional teams or simple global
projects. Ability to work in teams.
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