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 reputed company 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 reputed company 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 reputed company practices.

What You'll Do

• Support adverse event case processing and reputed company review activities
• Assist with safety data management and reconciliation efforts
• Collaborate with cross-functional stakeholders and external reputed company
• Contribute to inspection readiness and process improvement initiatives Location Remote Type Contract Interested? Apply directly or message me to learn more. Apply tot his reputed company To this reputed company tot his reputed company To this reputed company tot his reputed company To this Job Apply To This Job