Drug Safety Associate

Job Details:Creating and submitting adverse event and product complaint reports from data documented within our patient management system.Conduct quality check (QC) of information, spelling, drug, manufacturer and grammar included in the note.Communicating with clinicians regarding questions or concerns with the content or quality of adverse event reporting.Identify through the daily QC process and report any missing adverse events (AEs) and product complaints (PCs) to clinicians.Ensure that any identified missing reports have been submitted and accounted for.Maintain and submit weekly or monthly reconciliation reports to biopharma clients in accordance with client contracts.Assist clinical auditor in identifying trends or issues in adverse event reporting.Perform other duties as assigned.Qualifications/Requirements:Bachelor’s degree or commiserate experience preferred▪ Prior experience working in a Pharmacy setting preferred.Oncology experience a plus.Pharmacy technician or other clinical background preferred.Excellent written and verbal communication skills.Excellent organizational and time management skills.Competent in moderate to advanced computer skills.Competent in excel spreadsheets.Multi-task oriented.Ability to effectively work with people.Conscientious with excellent attention to detail.Flexible and adaptable.Essential to be able to type rapidly and accurately both numerical and text data.