Pharmacovigilance Associate

• Create and submit Adverse Event (AE) and Product Complaint (PC) reports from patient management system data• Conduct quality reviews of clinical documentation, ensuring accuracy in drug information, manufacturer details, spelling, and grammar• Communicate with clinicians regarding reporting questions and concerns• Identify and track missing AE/PC reports and ensure timely submission• Prepare and submit reconciliation reports for biopharma clients• Support clinical auditing activities and reporting process improvementsRequired Skills:• Excellent written and verbal communication skills• Strong organizational and time management abilities• Advanced computer proficiency, including Excel• Strong attention to detail and data entry accuracy• Ability to multitask and collaborate effectively with teamsPreferred Qualifications:• Bachelor's degree or equivalent experience• Experience in a pharmacy setting• Pharmacovigilance, Drug Safety, or Adverse Event Reporting experience• Oncology experience is a plus• Pharmacy Technician or clinical background preferred