Position Title: Pharmacovigilance Associate
Work Location: Cary, NC 27513
Assignment Duration: 5+ months (Potential Conversion)
Work Schedule: 9:00am-6:00pm eastern or 10:00am-7:00pm eastern
Work Arrangement: Remote, Candidate must be local to Cary, NC (Within 60 miles Radius).
1 week of onsite onboarding at Cary, NC, then 1 week of one-on-one training with Lead onsite. Then fully remote afterwards.
Position 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:
• 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.