Required to produce (research, write, edit, and review) high quality clinical, regulatory, scientific reports, manuscripts, and medical communication material including;

Writing clinical/regulatory documents such as clinical trial protocols, clinical study reports, investigator brochures, informed consent forms, clinical overviews and according to ICH or other guidelines

Publication manuscripts, abstracts, posters (content writing) and presentations

Other writing jobs and responsibilities assigned time to time

Develop templates for reports and other regulatory documents.

Take initiatives in process improvement areas