Medical writing
/ Medical literature review
Organization of a clinical trial and preparation of study-related
documentation are essential tasks. This complex activity includes revision and/or
translation/localisation of existing documents, or compilation of new ones from
background sources.
Competencies
- Clinical Development Plan
- Investigator's Brochure
- Study Protocol
- Case report form (CRF)
- Integrated Clinical Study Report
- Patient Information and Informed Consent Form for
biomedical research
- ICH CTD Clinical Part