Junior Pharmacovigilance Analyst

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

Job Summary

Join our dynamic team as a Junior Pharmacovigilance Analyst in the Pharma Research & Development sector. In this role, you will support activities related to the monitoring, evaluation, and analysis of drug safety data.

Working alongside cross-functional teams and internal stakeholders, you will assist with pharmacovigilance activities, case processing, safety reporting, and maintaining compliance with applicable regulatory requirements.

Responsibilities

• Support the monitoring and evaluation of adverse event reports in accordance with pharmacovigilance regulations and internal procedures.
• Assist with the analysis and communication of safety data.
• Support the preparation of safety reports and regulatory submissions.
• Assist with the maintenance and continuous improvement of pharmacovigilance systems and processes.
• Conduct literature reviews and surveillance activities to help identify potential safety signals and emerging risks.
• Support PV case processing, ensuring data quality, accuracy, and completeness.
• Assist with risk assessment and safety monitoring activities for pharmaceutical products.
• Maintain accurate documentation and records to support audits, inspections, and regulatory compliance.
• Participate in process improvement initiatives.
• Stay current with pharmacovigilance regulations, guidelines, and industry practices.

Qualifications

• Degree in a relevant scientific discipline such as Life Sciences, Pharmacy, Medicine, Nursing, or a related field.
• English level: C1+
• Exposure to or experience in Pharma Research & Development.
• Good analytical and problem-solving skills.
• Good communication and teamwork skills.
• Familiarity with risk management plans, safety assessments, and signal detection activities.
• Strong attention to detail and commitment to maintaining high-quality standards.
• Ability to work independently and manage multiple priorities