JOBSEARCHER

Pharmacovigilance Associate

Position Title:Pharmacovigilance AssociateAssignment Duration:6 months (Potential Conversion)Work Schedule:9:00am - 6:00pm eastern OR 10:00am - 7:00pm easternWork Arrangement:Candidate must be local to Cary, NC 27513 (within a 60 mile radius).1 week of onsite onboarding in Cary, NC1 week of one?on?one onsite training with the Lead, fully remote thereafterPosition Summary:Creating and submitting adverse event and product complaint reports from data documented within our patient management system.Key Responsibilities:* 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.Qualification & Experience:* 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.* 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.Mobile-Optimized JD SummaryAdverse Event Reporting Specialist (6-mo remote): Create/submit AE/PC reports, perform QC on notes, communicate with clinicians, reconciliation reports. Strong Excel + communication + detail required. 9-6 or 10-7 EST. (132 chars)