Junior Pharmacovigilance Analyst: Safety & Submissions

Cognizant; Argentina; On-site; ARS 600,000 - 1,000,000; Full time

Job summary

Cognizant in Argentina seeks a Junior Pharmacovigilance Analyst to support safety data monitoring, evaluation, and analysis within the Pharma Research & Development sector. You will assist PV case processing, regulatory submissions, and maintenance of PV systems while ensuring compliance with applicable standards.

Collaborating with cross-functional teams and stakeholders, you will conduct literature reviews, identify safety signals, and participate in process improvements to strengthen

Qualifications

• Degree in a scientific discipline related to pharmacovigilance or life sciences.
• English level C1+ requirement for communication with stakeholders.
• Exposure to Pharma R&D or pharmacovigilance activities is advantageous.

Responsibilities

• Support monitoring and evaluation of adverse event reports in line with PV regulations and procedures.
• Assist analysis and communication of safety data.
• Support preparation of safety reports and regulatory submissions.
• Maintain PV systems and processes and participate in process improvements.
• Conduct literature reviews and surveillance to identify safety signals and risks.
• Support PV case processing ensuring data quality and completeness.
• Assist risk assessment and safety monitoring for pharmaceutical products.
• Maintain documentation for audits and inspections.

Skills

English (C1+)

Analytical skills

Communication

Teamwork

Attention to detail

Independent work

Education

Life Sciences / Pharmacy / Medicine / Nursing or related field

Job description

Cognizant in Argentina seeks a Junior Pharmacovigilance Analyst to support safety data monitoring, evaluation, and analysis within the Pharma Research & Development sector. You will assist PV case processing, regulatory submissions, and maintenance of PV systems while ensuring compliance with applicable standards.

Collaborating with cross-functional teams and stakeholders, you will conduct literature reviews, identify safety signals, and participate in process improvements to strengthen