Job Title:
Associate Pharmacovigilance Specialist
Employer:
Clarivate
Locations:
Available in 2 locations
Department:
Life Sciences & Healthcare
Work Mode:
Hybrid (Monday – Friday)
Job ID:
JREQ133625
Posted Date:
September 15, 2025
Employment Type:
Full-Time | Permanent
About the Role:
The Associate Pharmacovigilance Specialist will support pharmacovigilance services by conducting biomedical literature monitoring and adverse event assessment for reporting purposes. The role requires broad knowledge of scientific terminology, medical concepts, drug safety regulations, and therapeutic areas.
You will be responsible for indexing, abstracting, and analyzing biomedical data, ensuring compliance with global pharmacovigilance standards while maintaining high accuracy and scientific integrity.
Key Responsibilities:
🔍 Monitor biomedical literature for relevant adverse event (AE) reports.
🧠 Assess and summarize case reports, studies, and specific biomedical topics.
🧾 Index and abstract key data for inclusion in pharmacovigilance systems.
💊 Apply comprehensive understanding of medical terminology, drugs, and therapeutic areas.
📚 Utilize commercial and client-specific literature databases to retrieve and evaluate safety information.
🤝 Collaborate with team members and adapt to evolving client requirements.
✍️ Support creation of accurate, concise, and clear summaries using scientific writing skills.
Education & Qualifications:
🎓 Required:
Master’s degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
OR degree in Dentistry, Physiotherapy, or Nursing (hospital-based patient exposure preferred)
🎓 Experience:
1–2 years of experience in biomedical literature review for AE reporting
OR equivalent combination of education + 1 year of relevant drug/patient safety experience
Related experience in Drug Safety / Pharmacovigilance (desirable)
Skills & Competencies:
🧩 Strong analytical ability to extract and summarize key findings from biomedical literature
✍️ Proven scientific writing skills for clear, precise summaries (min. 1 year experience)
💬 Excellent English communication (reading, writing, speaking, comprehension)
💊 Working knowledge of biomedical terminology, drugs, and therapeutic areas
💻 Experience using commercial and client-specific biomedical literature databases
🤝 Collaborative, adaptable, and able to work independently
💡 Detail-oriented with strong problem-solving mindset
🧠 Basic computer literacy
Preferred Qualifications: (Nice to Have)
📜 Certification from a professional medical writers association
🧠 Prior scientific/medical writing background
💻 Advanced experience with biomedical literature databases
Work Schedule:
🗓️ Monday to Friday
🏠 Hybrid Work Mode
Additional Information:
This job description provides a general overview of responsibilities. As business needs evolve, duties may be modified or expanded.
Equal Opportunity Statement:
Clarivate is an Equal Opportunity Employer, committed to fair employment practices and compliance with all applicable non-discrimination laws. All qualified applicants will receive consideration for employment regardless of race, color, religion, gender, age, national origin, disability, or any other protected status.
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