Job Title:
Associate Pharmacovigilance Specialist
Job Category:
Life Sciences & Healthcare
Location:
Remote / Hybrid (Available in 2 locations)
Job ID:
JREQ133625
Posted Date:
September 15, 2025
Job Purpose:
Perform pharmacovigilance services including biomedical literature monitoring, adverse event assessment, reporting, indexing, and abstracting, leveraging knowledge of medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Primary Responsibilities:
Review biomedical literature for adverse event reporting.
Index and abstract biomedical case reports and studies accurately.
Assess adverse events and prepare concise, accurate summaries.
Utilize broad knowledge of medical terminology, drugs, and therapeutic areas.
Maintain compliance with pharmacovigilance regulations and client-specific requirements.
Collaborate effectively with team members while maintaining the ability to work independently.
Adapt to changing client needs and project priorities.
Support creation of pharmacovigilance documentation with high-quality scientific writing.
Required Qualifications:
Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
Degree in Dentistry, Physiotherapy, or Nursing (hospital-based experience preferred).
1–2 years of experience reviewing biomedical literature for adverse event reporting or equivalent combination of education and experience.
Working knowledge of biomedical terminology, drugs, and therapeutic areas.
Strong analytic skills to summarize biomedical case reports and studies.
Excellent English comprehension, speaking, reading, and writing skills.
Experience with commercial and client-specific biomedical literature databases.
Basic computer literacy.
Preferred Qualifications:
Certification from a professional medical writer’s association.
Scientific or medical writing experience.
Prior exposure to drug safety or pharmacovigilance operations.
Skills & Competencies:
Analytical and critical thinking.
Attention to detail and accuracy.
Flexibility and adaptability to client requirements.
Ability to work independently and collaboratively.
Effective communication and documentation skills.
Work Hours:
Monday to Friday – Hybrid work mode
Other Information:
Additional duties may be assigned as business needs evolve.
Clarivate is committed to equal employment opportunities in all aspects of employment, including hiring, compensation, promotion, and training.
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