Senior Associate, Pharmacovigilance - Mexico - Remote

What the Senior Associate, Pharmacovigilance does WorldwideResponsible 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.Independently serves as Lead PV Associate on large sized studies/programs that are moderate to complex in scope of work.What you will doAuthor Safety Management Plan for assigned studiesReview incoming SAE data for completeness and accuracyPerform data entry in the Safety Database and/or complete applicable tracking of incoming safety informationGenerate queries for missing or unclear information and follow-up with sites for resolutionPerform QC of SAEs processed by other PV AssociatesGenerate regulatory reports and perform safety submissions as neededWhat you will bring to the roleExcellent understanding of medical and scientific terminology, of the principles of clinical a...