Cognizant Hiring Junior Data Analyst

Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant (a member of the NASDAQ-100 and one of Forbes World’s Best Employers 2024) is consistently listed among the most admired companies in the world.

Post : Junior Data Analyst (1 to 4 years experience into Pharmacovigilance)

Job Description
1. Triage & intake of ICSRs in ARGUS databases within agreed timelines
2. Download and monitor valid ICSRs from EudraVigilance (EV)- or any other sources
3. Process literature, spontaneous, clinical trial, and solicited cases
4. Search for valid ICSRs in Literature search tools
5. Generate reports and submit to health authorities and business partners
6. Enter serious and non-serious ICSRs in ARGUS per client SOP and WI with high accuracy
7. Code events, indications, patient history using MedDRA
8. Code suspect products, amend narratives, and label events
9. Obtain follow-up information for all cases per applicable guidelines
10. Submit processed cases to regulatory authorities and distribute reports to Partners

11. Communicate effectively with client stakeholders and internal teams
12. Attend all internal and client trainings to ensure guideline compliance
13. Ensure adherence to regulatory requirements and industry standards in all aspects of pharmacovigilance and safety operations.
14. Assist in the development and maintenance of standard operating procedures to ensure consistency and quality in process execution.
15. Support training and development initiatives to enhance team capabilities and knowledge in pharmacovigilance and safety operations.
16. Utilize technical skills to troubleshoot and resolve process-related issues, minimizing disruptions and ensuring smooth operations.
17. Engage in rotational shifts to provide consistent support and coverage across different time zones.

Candidate Profile
1. Bachelor’s / Master’s degree in pharmacy.
2. Minimum 1+ years relevant work experience in case processing activities.
3. Experience in Cardiovascular (CVS), Neuroscience (CNS), Oncology, Immunology therapeutic areas and Gene Therapy will be an added advantage. Experience with global pharma sponsor will be preferred.
4. In-depth knowledge and understanding of applicable global, regional, and local regulatory requirements, including Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and International Conference of Harmonization (ICH) guidelines, SOPs.
5. Excellent organizational and time management skills.
6. Proficiency in Microsoft Office and web-based applications (e.g., Word, Excel, PowerPoint).
7. Good knowledge of medical terminology.
8. Proven ability to follow instructions and guidelines, work independently, and take initiative.
9. Excellent attention to detail and accuracy in maintaining high-quality standards.
10. Strong written and verbal communication skills.

Additional Information
Experience : Minimum 1+ years
Qualification : B.Pharm, M.Pharm
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Pharmacovigilance
End Date : 10th July 2026