Pharmacovigilance Analyst

Job Summary

Join our dynamic team as a Pharmacovigilance Analyst in the Pharma Research & Development sector. In this role, you will play a critical part in ensuring the safety and efficacy of pharmaceutical products through the monitoring, evaluation, and analysis of drug safety data. Working closely with cross-functional teams, regulatory authorities, and internal stakeholders, you will support pharmacovigilance activities and contribute to maintaining compliance with global regulatory requirements.

Responsibilities

• Monitor and evaluate adverse event reports to ensure compliance with pharmacovigilance regulations and internal procedures.
• Collaborate with cross-functional teams to analyze, interpret, and communicate safety data effectively.
• Prepare safety reports and support regulatory submissions in accordance with applicable guidelines and timelines.
• Assist in the development, maintenance, and continuous improvement of pharmacovigilance systems and processes.
• Conduct literature reviews and surveillance activities to identify potential safety signals and emerging risks.
• Support PV case processing activities while ensuring data quality, accuracy, and completeness.
• Contribute to 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 to enhance operational efficiency and effectiveness.
• Stay current with pharmacovigilance regulations, industry trends, and best practices.

Qualifications

• Degree in a relevant scientific discipline such as Life Sciences, Pharmacy, Medicine, Nursing, or a related field.
• Experience in Pharma Research & Development.
• Strong analytical and problem-solving skills with the ability to interpret complex safety data.
• Proficiency in pharmacovigilance data management and safety databases.
• Excellent communication and teamwork skills, with the ability to collaborate across multiple stakeholders.
• Experience in PV Case Processing.
• Certification in Pharmacovigilance or Drug Safety Management is preferred.
• Familiarity with risk management plans, safety assessments, and signal detection activities.
• Up-to-date knowledge of pharmacovigilance regulations, guidelines, and industry standards.
• Ability to mentor and support junior team members.
• Strong attention to detail and commitment to maintaining high-quality standards.
• Ability to work independently and manage multiple priorities in a fast-paced environment.

Work Model

We believe hybrid work is the way forward as we strive to provide flexibility wherever possible. Based on this role's business requirements, this is a hybrid position requiring 2–3 days a week in a Cognizant office in Buenos Aires, Argentina. Regardless of your working arrangement, we are here to support a healthy work-life balance through our various wellbeing programs.

Benefits

• A career in one of the largest and fastest-growing IT services providers worldwide.
• Ongoing support and funding with training and development plans.
• Opportunity to work for leading global companies.
• A diverse, collaborative, and inclusive work environment.
• Highly competitive salary and benefits, including OSDE for you and your primary family group, annual bonus, and more.

Certifications Required

• Certification in Pharmacovigilance or Drug Safety Management (preferred).