Senior PV Analyst: ICSR & Global Safety Reporting

Advity Research; United States; On-site; USD 70,000 - 100,000; Full time

Job summary

A leading pharmaceutical research firm is in search of a professional with 3-4 years of pharmacovigilance experience. The role involves managing case processing of drugs and devices, conducting quality control reviews, and ensuring compliance with regulatory requirements. The ideal candidate will possess extensive medical terminology knowledge and excellent communication skills in English. This position offers the opportunity to work closely with global teams on critical safety processes.

Qualifications

• Minimum of 3-4 years of experience in pharmacovigilance including ICSR.
• Extensive knowledge of medical terminology and clinical pharmacology.
• Excellent communication skills in professional English.
• Sound knowledge of pharmacovigilance principles and international regulations.

Responsibilities

• Manage case processing for drugs, devices, vaccines, and cosmetics.
• Conduct QC review of literature searches and ICSR activities.
• Report IC.S.Rs and submit deliverables to clients.
• Maintain ICSR and related trackers.
• Provide queries for additional information needed in IC.S.Rs.

Job description

A leading pharmaceutical research firm is in search of a professional with 3-4 years of pharmacovigilance experience. The role involves managing case processing of drugs and devices, conducting quality control reviews, and ensuring compliance with regulatory requirements. The ideal candidate will possess extensive medical terminology knowledge and excellent communication skills in English. This position offers the opportunity to work closely with global teams on critical safety processes.