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Clarivate is inviting applications for the role of Associate Pharmacovigilance Specialist in its Life Sciences & Healthcare division. This is a fantastic opportunity for talented individuals with a background in life sciences and a passion for pharmacovigilance to join a global leader in healthcare information solutions.
Associate Pharmacovigilance Specialist
Locations: 2 (Hybrid – Remote Option Available)
Department: Life Sciences & Healthcare
Job ID: JREQ133625
About the Role
As an Associate Pharmacovigilance Specialist, you will be responsible for providing high-quality pharmacovigilance services such as:
- Monitoring biomedical literature and identifying adverse events for reporting
- Indexing and abstracting scientific publications
- Applying scientific knowledge and pharmacovigilance regulations to ensure accuracy and compliance
This role demands strong analytical skills, attention to detail, and the ability to summarize complex biomedical information clearly and precisely.
Education & Experience Requirements
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences
(Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.) - A degree in Dentistry, Physiotherapy, or Nursing with hospital-based patient exposure is an added advantage.
- 1–2 years of experience in reviewing biomedical literature for adverse event reporting
(OR an equivalent combination of education and relevant experience) - Prior experience in drug safety/pharmacovigilance is desirable.
Key Skills & Competencies
- Strong analytical ability to evaluate and summarize biomedical case reports and studies
- At least 1 year of experience in scientific/medical writing
- Working knowledge of biomedical terminology, drugs, and therapeutic areas
- Excellent command of the English language (reading, writing, speaking, comprehension)
- Familiarity with commercial and client-specific biomedical literature databases
- Ability to work independently as well as collaboratively
- Flexibility to adapt to changing client needs
- Basic computer literacy
Preferred Qualifications
- Certification from a professional medical writer’s association
- Scientific or medical writing background
- Additional experience with biomedical databases
Why Join Clarivate?
- Work with a global leader at the forefront of drug safety and medical research.
- Hybrid work model for improved work-life balance.
- Opportunities for career advancement and continuous learning.
- Make a meaningful impact on patient safety and global healthcare.
How to Apply
Interested candidates can apply through Clarivate’s official career portal using Job ID: JREQ133625.
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