Fortrea Pharmacovigilance Hiring | Safety Science Coordinator II

Safety Science Coordinator II – Fortrea (2–3 Years Experience, Bangalore)

Safety Science Coordinator II – Pharma, 2-3 Yrs, Bangalore
Apply for Safety Science Coordinator II at Fortrea, Bangalore. Pharma/Life Sciences graduates with 2–3 years drug safety experience.

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Looking for an exciting opportunity in drug safety and pharmacovigilance? Fortrea is inviting applications for the role of Safety Science Coordinator II at its Bangalore location. This position is ideal for professionals with 2–3 years of experience in pharmacovigilance or clinical trial case processing who are eager to contribute to global clinical safety operations.

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Company Overview

Fortrea is a global leader in clinical research and drug development services, working closely with pharmaceutical and biotechnology organizations worldwide. With a mission to deliver safer and more effective therapies, Fortrea is recognized for its innovation, regulatory expertise, and dedication to advancing healthcare.

As a trusted partner in the life sciences industry, Fortrea provides end-to-end support in clinical development, patient safety, and data-driven insights—helping shape the future of drug safety and pharmacovigilance.

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Job Role & Responsibilities

As a Safety Science Coordinator II, you will be responsible for ensuring compliance and quality in pharmacovigilance and clinical safety operations. Your role will involve:

• Adverse Event Case Processing

  • Receipt, review, and entry of AE/SAE reports from clinical trials or spontaneous sources.

  • Writing patient narratives and coding adverse events using MedDRA.

  • Identifying missing or clinically significant data and generating queries for collection.

• Regulatory Submissions & Reporting

  • Submitting expedited SAE reports to clients, regulatory authorities, ethics committees, and investigators.

  • Managing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).

  • Ensuring timelines for safety submissions are strictly met.

• Quality Management & Documentation

  • Maintaining project files, central documentation, and adverse event tracking systems.

  • Supporting database reconciliation and quality review of processed reports.

  • Assisting in preparation for audits and regulatory inspections.

• Training & Collaboration

  • Mentoring junior pharmacovigilance staff.

  • Coordinating with internal stakeholders, clients, and regulatory agencies.

  • Participating in client meetings and contributing to project metrics and monthly reports.

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Eligibility / Qualifications

Essential:

• Bachelor’s or Master’s degree in Pharmacy, Biological Sciences, Nursing, Medical Sciences, Life Sciences, or related fields.

• 2–3 years of drug safety experience with exposure to clinical trial case processing.

Desirable Skills:

• High accuracy and attention to detail in pharmacovigilance case handling.

• Strong knowledge of MS Office and safety databases.

• Excellent written and verbal communication skills.

• Ability to work independently with minimal supervision.

• Mentoring and leadership skills are a plus.

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Location & Salary

• Location: Bangalore, India

• Work Mode: Hybrid (office environment with flexibility)

• Compensation: Competitive salary with benefits aligned to global CRO industry standards

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Application Process

Interested candidates can apply directly through the official Fortrea career portal:
👉 Apply Here

📅 Application Deadline: 28 September 2025

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Why Join Fortrea?

• Be part of a global leader in clinical safety and drug development.

• Work on cutting-edge projects ensuring patient safety across markets.

• Gain exposure to international pharmacovigilance regulations and practices.

• Grow your career with continuous learning, mentoring, and professional development.

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FAQs

Q1: Who can apply for this position?
Candidates with a degree in Pharmacy, Life Sciences, Medical Sciences, or Nursing and at least 2–3 years of pharmacovigilance/drug safety experience can apply.

Q2: What kind of work environment does Fortrea offer?
Fortrea offers a hybrid work model with an office base in Bangalore, ensuring both flexibility and team collaboration.

Q3: Is prior clinical trial experience mandatory?
Yes, exposure to clinical trial case processing is required for this role.

Q4: What software skills are needed?
Working knowledge of pharmacovigilance databases, MedDRA coding, and MS Office tools is required.

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Summary Table