Description

Create Medical/Safety/clinical documents (Investigator brochure, report, Medical section of CTA etc) Monitor the execution of strategic regulatory/labelling documents Review medical & scientific literature Reviews for grammar, format and consistency Required Candidate profile Master's in Life science/Mpharm Exp 2 years medical writing Good knowledge of drug development, medical writing & associated regulations Knowledge of statistical principles & medical terminology Role: Medical Writer Industry Type: IT Services & Consulting Department: Research & Development Employment Type: Full Time, Permanent Role Category: Pharmaceutical & Biotechnology

Role and Responsibilities

• Create Medical/Safety/clinical documents (Investigator brochure, report, Medical section of CTA etc) Monitor the execution of strategic regulatory/labelling documents Review medical & scientific literature Reviews for grammar, format and consistency Required Candidate profile Master's in Life science/Mpharm Exp 2 years medical writing Good knowledge of drug development, medical writing & associated regulations Knowledge of statistical principles & medical terminology Role: Medical Writer Industry Type: IT Services & Consulting Department: Research & Development Employment Type: Full Time, Permanent Role Category: Pharmaceutical & Biotechnology