Junior Pharmacovigilance Analyst

Cognizant; Buenos Aires; On-site; ARS 600,000 - 900,000; Full time

Job summary

Cognizant in Argentina is seeking a Junior Pharmacovigilance Analyst to support drug safety activities within Pharma R&D. You will assist with case processing, safety reporting, and regulatory submissions, collaborating with cross-functional teams to ensure compliance.

Ideal candidates have a Life Sciences related degree, strong analytical and communication skills, and the ability to manage multiple priorities.

Qualifications

• English level: C1+
• 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 high-quality standards
• Ability to work independently and manage multiple priorities

Responsibilities

• Support monitoring and evaluation of adverse event reports per regulations and procedures
• Assist analysis and communication of safety data
• Help prepare safety reports and regulatory submissions
• Maintain and improve pharmacovigilance systems and processes
• Conduct literature reviews and surveillance to identify safety signals and risks
• Support PV case processing with data quality and completeness
• Assist risk assessment and safety monitoring for pharmaceutical products
• Maintain documentation for audits, inspections, and regulatory compliance
• Participate in process improvement initiatives
• Stay current with PV regulations and industry practices

Skills

English (C1+)

Analytical thinking

Communication & teamwork

Risk management & safety

Attention to detail

Independent work & prioritization

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

Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.