Latest M Pharm Jobs at Clarivate | Apply Now for Pharmacovigilance Role
Are you looking for a career in pharmacovigilance that combines science, research, and patient safety? Clarivate is hiring an Associate Pharmacovigilance Specialist (Hybrid) to join its global team in Life Sciences & Healthcare. In this role, you will support pharmacovigilance services through biomedical literature monitoring, adverse event reporting, indexing, and abstracting—helping ensure the highest standards of drug safety and compliance.
About the Company
Clarivate is a trusted global leader in data-driven insights, technology, and innovation across life sciences, healthcare, and beyond. With a mission to accelerate innovation and improve patient outcomes, Clarivate provides solutions that empower researchers, regulators, and healthcare professionals to make informed decisions that shape the future of medicine and global healthcare.
Job Details
- Job Title: Associate Pharmacovigilance Specialist
- Job ID: JREQ133625
- Department: Life Sciences & Healthcare
- Schedule: Monday to Friday
- Work Mode: Hybrid
Qualifications & Skills
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Education:
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Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
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A degree in Dentistry/Physiotherapy/Nursing (hospital-based experience) is an advantage.
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Experience:
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1–2 years reviewing biomedical literature for adverse event reporting or equivalent combination of education/experience.
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Knowledge of pharmacovigilance and drug safety processes preferred.
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Strong analytical ability to evaluate biomedical reports and summarize key findings.
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1+ years of biomedical terminology, drugs, and therapeutic area experience.
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Prior use of biomedical literature databases.
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Skills:
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Excellent English (reading, writing, speaking, comprehension).
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Strong scientific/medical writing ability.
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Flexibility, adaptability, and the ability to work independently or in teams.
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Basic computer literacy.
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Preferred:
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Certification from professional medical writers’ associations.
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Experience in scientific/medical writing.
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Key Responsibilities
- Perform pharmacovigilance services including biomedical literature monitoring, adverse event assessment, reporting, and indexing.
- Review, analyze, and summarize biomedical case reports, studies, and therapeutic topics.
- Create accurate, succinct, and precise abstracts of biomedical literature.
- Support drug and patient safety teams with pharmacovigilance insights.
- Adapt to evolving client needs while ensuring compliance with pharmacovigilance regulations.
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