Pharmacovigilance Associate (Contract) | Remote

• 6-month contract, extension or conversion to FTE available
• 40 hours/week

We're partnering with an innovative biotech organization seeking a Pharmacovigilance Associate to support day-to-day drug safety operations. This role is ideal for someone with early-career pharmacovigilance experience who is looking to expand their expertise in case processing, safety systems, and regulatory compliance within a fast-paced environment. Key Qualifications:

• 1-3 years of pharmacovigilance or drug safety experience
• PharmD preferred
• Hands-on ICSR case processing and QC experience
• Experience in safety databases, including end-to-end case workflow (intake through submission/distribution), case follow-up, and data quality activities.
• Working knowledge of global PV regulations and guidelines (e.g., ICH E2A/E2B(R3)/E2D; FDA/EMA reporting concepts) and pharmacovigilance SOPs.
• Experience with medical coding conventions and safety data quality practices.

What You'll Do:

• Support adverse event case processing and quality review activities
• Assist with safety data management and reconciliation efforts
• Collaborate with cross-functional stakeholders and external partners
• Contribute to inspection readiness and process improvement initiatives

Location: Remote Type: Contract Interested? Apply directly or message me to learn more.