Job Description
The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
About You - Education, Experience, Skills
Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).Fresher / Upto 2 years of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety)Strong analytic ability to analyse and summarize the main points of biomedical case reports, studies, or specific topics.Working knowledge of biomedical terminology, drugs...
Ready to Apply?
Take the next step in your AI career. Submit your application to Clarivate today.
Submit Application