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 r