Statistical Pharma

Regulatory affairs specialist job description Exact responsibilities may vary depending on the company, but as a general rule you will: Provide regulatory expertise to scientists and senior management on new product development, and assist with the preparation and submission of…

Key ResponsibilitiesProvide clinical study start up expertise.Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent formsTrack IRB submissionsCollect, review, and process essential documents and identify issues that site needs to…