Pharmacovigilance Associate

Position Title: Pharmacovigilance Associate

Assignment Duration: 6 months (Potential Conversion)

Work Schedule: 9:00am - 6:00pm eastern OR 10:00am - 7:00pm eastern

Work Arrangement: Candidate must be local to Cary, NC 27513 (within a 60?mile radius).

1 week of onsite onboarding in Cary, NC

1 week of one?on?one onsite training with the Lead, fully remote thereafter

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:

* 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 Summary Adverse 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)