Safety Science Analyst Vacancy at Fortrea (Bangalore) – Freshers Can Apply!

Fortrea, a global leader in clinical research solutions, is inviting applications for the position of Safety Science Analyst at its Bangalore location. This is an excellent opportunity for fresh graduates or professionals with up to 6 months of experience in life sciences or healthcare domains to step into the dynamic field of pharmacovigilance and drug safety.

📅 Important Dates:

• Position Type: Full-Time (Contractual – 6 Months)

• Location: Bangalore, India

• Application Deadline: June 21, 2025

• Job Requisition ID: 253053

📝 Job Overview:

As a Safety Science Analyst, you will play a critical role in managing and processing adverse event data from clinical trials and post-marketing surveillance. The role supports compliance with global regulatory standards while ensuring accurate and timely safety reporting to clients and authorities.

🔍 Key Responsibilities:

• Triage and intake of safety information from various sources

• Enter safety data into adverse event tracking systems

• Write clear, medically accurate patient narratives

• Code adverse events using MedDRA

• Perform listedness assessments (for marketed products)

• Generate and resolve queries in coordination with medical teams

• Submit expedited SAE reports to regulatory authorities, ethics committees, and clients

• Assist with periodic safety report submissions and database reconciliation

• Maintain and archive project and case documents as per SOPs

• Support quality management and ensure operational compliance

🎓 Qualifications:

• Educational Background: Degree in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or a related discipline

• Experience: 0 to 6 months of relevant experience. Internship or academic exposure in safety reporting or clinical data management is a plus.

Candidates with equivalent relevant experience in medical affairs, regulatory affairs, clinical data monitoring, or QA may also be considered.

🧠 Skills & Competencies:

• Strong attention to detail and analytical mindset

• Proficient in MS Office applications

• Good communication and writing skills

• Ability to manage and proofread numerical and clinical data

• Team-oriented with the ability to collaborate across departments

• Familiarity with safety reporting guidelines and pharmacovigilance practices is beneficial

🏢 Work Environment:

This is an office-based role located in Bangalore. The position supports global clinical safety operations and requires strong coordination with internal and external stakeholders.

💡 Why Join Fortrea?

• Get hands-on experience in clinical safety and pharmacovigilance

• Collaborate with global industry leaders

• Contribute to projects that impact patient safety worldwide

• Receive exposure to international regulatory standards and systems

• Begin a promising career path in the pharmaceutical and clinical research industry

⏳ Apply Before: June 21, 2025

Kickstart your career in clinical research and drug safety. Apply now and become a part of a passionate, mission-driven team at Fortrea!

APPLY HERE