Are you a professional with a background in life sciences and a passion for drug safety? Fortrea, a leading global Contract Research Organization (CRO), is currently hiring for the position of Specialist I at their Bangalore hub. This is a critical role within the Patient Safety Solutions (PSS) department, focusing on the end-to-end management of adverse event reporting for both clinical trials and post-marketing surveillance.
With the application deadline fast approaching on April 30, 2026, now is the perfect time to explore how your expertise in pharmacovigilance can contribute to global patient health.
Role Overview: What Does a Specialist I Do?
The Specialist I is responsible for the overall operational support of clinical safety. This involves the meticulous processing of adverse events (AEs) to ensure they meet the highest standards of quality and regulatory compliance. You will act as a guardian of patient safety, ensuring that any potential risks associated with pharmaceutical products are identified, documented, and reported to regulatory agencies within strict timelines.
Core Responsibilities:
- Adverse Event Case Management: Handle receipt, data entry, and processing of AE reports
- Medical Coding & Narratives: Use MedDRA for accurate coding and write detailed narratives ✍️
- Expedited Reporting: Submit urgent cases to global regulatory authorities
- Safety Database Maintenance: Track, reconcile, and ensure listedness
- Regulatory Submissions: Support PSUR and DSUR preparation
- Quality Assurance: Maintain accuracy through reviews
- Mentorship: Support junior staff 🤝
Who Should Apply? Eligibility & Qualifications
Educational Requirements:
- Bachelor’s/Master’s in Life Sciences, Pharmacy, Nursing
- PharmD candidates preferred
Experience:
- BS/BA: 1–2 years safety / 2–3 years relevant experience
- MS/MA/PharmD: 1–2 years safety / 2 years relevant
- Non-degree: 4–5 years relevant experience
Key Skills:
- Attention to detail 🔍
- Knowledge of ICH Guidelines & GCP
- Technical proficiency
- Strong communication skills
How to Apply
Interested candidates should visit the official Fortrea careers portal and search for Requisition ID: 26731. Ensure your CV clearly highlights your experience in AE/SAE processing, MedDRA coding, and safety database handling. Apply before April 30, 2026 to secure your chance.
Why Work at Fortrea in Bangalore?
- Professional Growth: Exposure to advanced pharmacovigilance processes
- Global Impact: Work on international regulatory projects
- Career Progression: Opportunities to move into senior roles
Application Details 📅
- Location: Bangalore, India 📍
- Job ID: 26731
- Employment Type: Full-time
- Deadline: April 30, 2026
Essential Safety & Health Compliance
Employees must follow global safety and compliance standards aligned with international guidelines, ensuring both patient and workplace safety.
