Proficiency in pharmacovigilance data management. Degree in a relevant scientific discipline. Collaborate with cross-functional teams to analyze and interpret……
Understanding and presenting complex scientific and clinical research data and analysis methodologies. Working and managing individuals and data to drive……
Run timely subject visit completion reports and enter data into CTMS. Graduated - Bachelor’s degree in appropriate scientific or business disciplines.…
Understanding and presenting complex scientific and clinical research data and analysis methodologies. Working and managing individuals and data to drive……
Understanding and presenting complex scientific and clinical research data and analysis methodologies. Working and managing individuals and data to drive……
Understanding and presenting complex scientific and clinical research data and analysis methodologies. Working and managing individuals and data to drive……
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About the role
As a Pharmacovigilance Analyst, you will make an impact by ensuring the safety and efficacy of pharmaceutical products through monitoring and evaluation of drug safety data. You will be a valued member of the IOA team and work collaboratively with cross-functional teams, regulatory bodies, and internal stakeholders. In this role, you will:
Monitor and evaluate adverse event reports to ensure compliance with regulatory requirements.
Collaborate with cross-functional teams to analyze and interpret safety data.
Prepare safety reports and assist with regulatory submissions.
Support the development and maintenance of pharmacovigilance systems and processes.
Conduct literature reviews to identify potential safety signals. Work model
Based on this role’s business requirements, this is a hybrid position in Argentina , with work conducted from a Cognizant office, CABA, Buenos Aires. Work shift
Monday to Friday, 9:00 AM – 6:00 PM (local time) we need to work approximately half of the public holidays each year What you need to have to be considered
Degree in a relevant scientific discipline.
English and Spanish proficiency at C1 level or higher (mandatory) , as trainings and cross‑functional collaboration are conducted primarily with global teams based in India and the United States .
6 months to 1 year of experience in Pharma Research & Development.
Strong analytical and problem-solving skills.
Proficiency in pharmacovigilance data management.
Excellent communication and teamwork abilities. These will help you stand out
Experience in PV Case Processing.
Certification in Pharmacovigilance or Drug Safety Management.
Familiarity with risk management plans and safety assessments.
Ability to mentor junior team members.
Up-to-date knowledge of pharmacovigilance regulations and guidelines. 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.