The medical writer should research, and prepare study protocols in the required format.
. The medical writer is responsible for researching, writing and editing clinical/statistical reports and study protocols, and summarizing data from clinical studies for submission to the regulatory body.
Handle editorial review and change for assigned documents.
Initiate document writing for regulatory submissions.
Assess and edit analysis plans.
Conduct on-line literature search.
Function as primary functional representative on project teams.
Interface with clients and engage in client meetings.
Job Type: Full-time