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 improvements

Required 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 teams

Preferred 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