About the role
Position Title:
Pharmacovigilance Associate
Assignment Duration:
4+ 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.
Background & Context:
Supports pharmacovigilance reporting and quality checks for The Organization.
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
- Prior experience with pharmacovigilance strongly 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.
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