Pharmacovigilance Jobs in Bangalore- Join the Fortrea Careers Team | Apply Now
Are you ready to take the next step in your pharmacovigilance career? Fortrea is offering exciting Pharmacovigilance Jobs for skilled professionals in Bangalore. As a Safety Science Coordinator II, you’ll contribute to patient safety by managing clinical safety operations, analyzing adverse event data, and ensuring compliance with global health regulations. Join Fortrea Careers and make an impact, where numerous rewarding pharmacovigilance jobs await, in advancing healthcare worldwide.
- Job Position: Safety Science Coordinator II
- Location: Bangalore, India
- Job ID:25692
- End Date to Apply: November 2, 2025
About the Company
Fortrea is a global leader in clinical development and patient safety services, delivering innovative solutions that drive healthcare progress. The company partners with leading pharmaceutical and biotech organizations to ensure the safety, efficacy, and regulatory compliance of their medical products. Through Fortrea Careers, professionals get the chance to work on groundbreaking research that impacts millions of lives worldwide, especially in various roles related to pharmacovigilance jobs.
Job Description
Fortrea is seeking a Safety Science Coordinator II to support global clinical and post-marketing safety operations. In this role, you’ll be responsible for processing adverse events, maintaining regulatory compliance, and ensuring timely reporting across multiple projects. This opportunity offers a dynamic environment for those pursuing excellence in various pharmacovigilance job roles.
Key Responsibilities in Pharmacovigilance Jobs
- Process adverse event reports from all sources per client and sponsor agreements.
- Manage receipt, review, and data entry of safety data into regulatory databases.
- Write patient narratives and accurately code adverse events using MedDRA.
- Identify missing clinical data and generate follow-up queries.
- Ensure expedited reporting to clients and regulatory authorities within set timelines.
- Handle ESRs and PSRs and maintain documentation per SOPs.
- Support peer reviews, audits, and team training activities.
- Maintain project-level documentation and ensure data quality and compliance.
- Assist in client communication, meetings, and regulatory submissions. These tasks are essential for those engaged in pharmacovigilance jobs.
Qualifications for Fortrea Pharmacovigilance Job
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, or Medical Sciences.
- 2–3 years of relevant experience in pharmacovigilance or clinical trial case processing.
- Strong attention to detail and commitment to data accuracy.
- Excellent communication and teamwork skills.
- Proficient in MS Office and familiar with clinical safety systems.
- Mentoring or team support experience preferred.
Link to Original Notification to apply: APPLY ONLINE HERE
