Job Profile: Medical Writer
Location: India - Karnataka - Bengaluru
Post-graduate degree in life sciences or equivalent expertise
Preferable 1 - 3 years of clinical regulatory writing experience in the pharmaceutical industry
Possesses a good understanding of basic drug development.
Demonstrates knowledge of scientific methodology in the design, conduct, and description of clinical research.
Ability to author clinical regulatory documents following defined templates.
Demonstrates an understanding of how to interpret and describe clinical data.
Understands the organization of clinical study reports and other documentation.
Possesses working knowledge of International Committee for Harmonisation (ICH) / Good Clinical Practice (GCP).
Possesses good working knowledge of statistical principles used in clinical research
Possesses necessary computer skills and general computer literacy.
Excellent English language skills (verbal and written)