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) Related experience in drug safety/ pharmacovigilance is desirable. Strong analytic ability to analyse and summarize the main points of biomedical case reports, studies, or specific topics. Working knowledge of biomedical terminology, drugs, and therapeutic areas. Experience with commercial and client-specific biomedical literature databases.

It would be great if you also had . . .

Certification from a professional medical writer's association Experience with commercial and client-specific biomedical literature databases Scientific/medical writing background A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage.

Work hours

Monday to Friday (Hybrid work model) 12PM - 9 PM


At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.