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Cognizant ICSR Jobs | Pharmacovigilance Roles Mumbai & Hyderabad |

If you’re looking to advance your career in pharmacovigilance (PV), this latest opening for ICSR Case Processing Associate at Cognizant offers a strong opportunity to work on global drug safety projects. With demand rising for skilled professionals in ICSR processing jobs in India, this role is ideal for candidates with hands-on experience in safety databases and regulatory compliance.


Cognizant, a globally established organization, is hiring experienced candidates for pharmacovigilance jobs in Mumbai and Hyderabad, offering structured career growth and exposure to international regulatory standards.


Job Overview

Position: ICSR Case Processing Associate

Location: Mumbai, Hyderabad

Work Mode: Work from Office

Experience Required: Minimum 2 Years in ICSR Case Processing

Industry: Pharmacovigilance / Drug Safety

Employment Type: Full-Time


Key Responsibilities

As part of the ICSR case processing team, your responsibilities will include:


Processing and reviewing Individual Case Safety Reports (ICSRs)

Performing data entry and quality checks in safety databases

Ensuring compliance with global regulatory guidelines (FDA, EMA, ICH)

Coding adverse events using MedDRA and WHO Drug Dictionary

Meeting productivity and quality benchmarks in PV operations

Collaborating with cross-functional teams for case resolution

Identifying and escalating potential drug safety concerns


Required Qualifications & Skills

To qualify for this ICSR processing role in India, candidates should have:


Degree: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences or related field)

Minimum 2 years of experience in pharmacovigilance / ICSR case processing

Hands-on experience with safety databases like Argus, ArisG, or Veeva

Strong knowledge of MedDRA coding and PV regulations

Excellent communication and documentation skills

High attention to detail and analytical ability

Ability to work in a deadline-driven environment


Salary & Benefits

Estimated Salary Range: ₹4,00,000 – ₹7,50,000 per annum

Exposure to global pharmacovigilance projects

Strong career growth in drug safety and regulatory domains

Continuous learning and upskilling opportunities

Stable work environment in a reputed MNC


Why Choose This Role?

With increasing global focus on drug safety and regulatory compliance, professionals with expertise in ICSR case processing are in high demand. This opportunity allows you to:


Work with a globally recognized organization

Gain exposure to international PV systems

Strengthen your profile in pharmacovigilance careers

Build long-term growth in clinical safety operations


How to Apply

Interested candidates can apply directly by sending their updated CV to:



Application Tips:


Highlight your ICSR experience and case volumes handled

Mention tools like Argus, Veeva, ArisG

Include productivity metrics and quality scores


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