Associate ii, pharmacovigilance – brazil – remote em alemanha (SE) – alemanha
Requisitos
Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to large sized studies that are moderate to complex in scope of work with moderate support from senior staff.
Author Safety Management Plan for assigned studies
Attend and present at Investigator Meetings
Review incoming SAE data for completeness and accuracy
Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
Perform QC of SAEs processed by other PV Associates
Generate regulatory reports and perform safety submissions as needed