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Fortrea Pharmacovigilance Opening | Safety Science

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Fortrea

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Nursing, Medical Sciences

Bangalore

2–3 years

Verified Job

Online Application
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Are you passionate about pharmacovigilance, clinical safety, and regulatory compliance?
Fortrea is hiring a Safety Science Coordinator II in Bangalore, India—a great opportunity for life science professionals with 2–3 years of experience in clinical trial case processing or safety data management.

This full-time role involves managing adverse event reports, ensuring timely submissions to regulatory bodies, and maintaining high-quality safety documentation. If you have a strong eye for detail and a background in pharmacy, medical sciences, or life sciences, this could be your next career move.


Key Responsibilities

As a Safety Science Coordinator II, you will:

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  • Process and manage adverse event reports from clinical trials and post-marketing sources.
  • Perform data entry, medical coding (MedDRA), and narrative writing for safety cases.
  • Identify missing or clinically significant data and raise follow-up queries.
  • Ensure compliance with global regulatory timelines for expedited reporting.
  • Submit safety reports to clients, regulatory authorities, and ethics committees.
  • Support database reconciliation, ESR/PSR preparation, and project file management.
  • Assist in audits, quality reviews, and staff mentoring.
  • Maintain study-level documentation and SOP compliance.

Qualifications and Experience

Education:

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

Experience:

  • 2–3 years of relevant experience in pharmacovigilance or clinical trial case processing.
  • Strong attention to detail and accuracy.
  • Proficient in MS Office and safety database systems.
  • Excellent communication skills and ability to work both independently and collaboratively.
  • Prior experience in adverse event data entry and reporting preferred.

Why Join Fortrea?

  • Work with a global leader in clinical research and pharmacovigilance.
  • Opportunity to enhance your expertise in drug safety and clinical operations.
  • Supportive team environment with hybrid work flexibility.
  • Competitive compensation and growth prospects in a dynamic healthcare sector.

How to Apply

Application Link

Fortrea Pharmacovigilance Opening | Safety Science
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