Pharmacovigilance Jobs at Fortrea Careers | Assistant Workflow Analyst Role
If you’re planning to build a strong career in pharmacovigilance, this opportunity with Fortrea is one of the most promising pathways in today’s competitive clinical research jobs market. As an Assistant Workflow Analyst II, you will support drug safety workflows, streamline case processing, and contribute to global pharmacovigilance systems—making this role an excellent entry-to-mid-level position for life science graduates aiming to step into the world of pharmacovigilance jobs.
- Position: Assistant Workflow Analyst II
- Locations: Pune
- Job Requisition ID: 255655
About the Company:
Fortrea is a leading global CRO that accelerates clinical development and enhances drug safety operations worldwide. With a strong footprint in clinical research and regulatory services, Fortrea offers dynamic career opportunities in drug safety, biometrics, and medical operations—making it an ideal environment for professionals seeking growth in Fortrea careers.
Job Overview:
The Assistant Workflow Analyst II will perform core drug safety and pharmacovigilance support activities, including case tracking, assignment, quality control support, and SLA monitoring. This position ensures smooth workflow operations and timely processing of safety cases across teams.
Educational Requirements:
- Bachelor’s in life sciences or related discipline
- B.S./B.A. with 6 months–2 years of relevant experience
- M.S./M.A. with 0–2 years of relevant experience
- Equivalent relevant experience may be considered
- MSCIT or equivalent certification is preferred
Key Responsibilities:
- Segregate safety cases based on priority, due dates, and SLAs
- Assign cases to case processing teams in consultation with Team Leads
- Maintain and update the master case tracking sheet
- Monitor case progression and ensure timely completion
- Perform daily reconciliation of received vs processed cases
- Support lead teams by updating productivity, QC, and workload trackers
- Assist with pharmacovigilance support tasks including data reconciliation
- Contribute to TAT monitoring and ensuring compliance with internal timelines
- Troubleshoot workflow challenges and coordinate with internal teams
Skills Required:
- Basic understanding of clinical research industry & ICH-GCP guidelines
- Knowledge of pharmacovigilance processes and safety databases
- Familiarity with ICSR types and regulatory timelines
- Proficiency in MS Office; Excel macro experience preferred
- Strong analytical, communication and coordination skills
- Ability to work in a fast-paced, deadline-driven environment
Important Dates:
- Application Deadline: November 24, 2025
This role is an excellent stepping stone for life science graduates and professionals aspiring to advance in pharmacovigilance jobs or transition into broader clinical research jobs. With Fortrea’s global environment, you’ll gain hands-on exposure to drug safety workflows and industry-standard PV systems—setting the foundation for a strong and rewarding career.
