Description
Main Duties Include:*The collection, maintenance, and processing of ICSRs (Individual Case Safety Reports)
*Writing and Updating of SOPs
*Database Entry and Analysis
*Reporting to Regulatory Authority and Ethics Comittees
*Quality Control
*Potential Training of non PV staff
Experience
*Minimum 2 Years experience in a Pharmacovigilance role
*Formal Education in Life Science or related topic
*Knowledge of EU Clinical Drug Safety environment
*Fluent Swedish and English communication skills
Next Steps
Please contact Samuel Bacon at Real Life Sciences by either contacting me directly on the phone number provided or submitting your CV via the link.
Mehr Informationen über Real Staffing erhalten Sie unter www.realstaffing.com/de