ob Title
Safety Science Coordinator – Pharmacovigilance
🔹 Eligibility Criteria
- Education: PharmD, MPharm, BPharm, or related qualifications in medical/life sciences.
- Experience: Minimum 1 year of relevant experience in safety data management, clinical research, or pharmacovigilance.
- Skills Required:
- Working knowledge of MedDRA and pharmacovigilance databases.
- Familiarity with global regulatory frameworks.
- Strong attention to detail, logical thinking, and excellent communication skills.
- Proficiency in English (written & spoken) and the local language.
- Computer proficiency with Microsoft Office tools.
🔹 Why Join Fortrea?
Fortrea is recognised worldwide as a trusted Contract Research Organisation (CRO), supporting clinical research and drug development across multiple therapeutic areas.
As part of the team, you will:
✔ Gain hands-on exposure to pharmacovigilance and safety data management.
✔ Develop expertise in regulatory compliance and clinical research operations.
✔ Build a strong career path with opportunities for growth and global exposure.
✔ Work in a collaborative, quality-focused environment.
📍 Job Location
Pune, Maharashtra – India
🔹 How to Apply
Interested candidates can apply directly via the Fortrea Careers Page or through trusted job portals like LinkedIn, Indeed, or Naukri.
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