Primary Location Europe

Job ID: PL_WA-2411

Job Type: Full-Time

JOB DESCRIPTION

Your main responsibilities:

• Assisting CRAs in their routine work
• Completing submission of documents to the Regulatory Authority (including safety reports) when required
• Reporting safety data to Sponsor’s Pharmacovigilance Department and providing assistance when required
• Performing remote monitoring and site management
• Collecting, reviewing and tracking regulatory documents when required
• Performing translations (only in case of appropriate education)
• Assisting with the completing of study specific documents, annotated Case Report Forms (CRFs), tracking forms, and other study related documents
• Participating in study specific training
• Providing status updates to CRAs and Project Manager
• Participating in the preparation and coordination of inve...