"Exciting Opportunity: Apply for Senior Pharmacovigilance Specialist Position at Clarivate Analytics!"

Clarivate Pharmacovigilance Jobs For Pharmacy – Apply Online

At Clarivate Analytics, we are currently looking for a Senior Pharmacovigilance Specialist to join our team. If you have experience in reviewing biomedical literature for adverse event reporting and a strong background in drug safety/pharmacovigilance, we encourage you to apply.

Position: Senior Pharmacovigilance Specialist

Reports To: Director, Consulting; Senior Manager, Pharmacovigilance; Manager, Pharmacovigilance

Organization: Clarivate Analytics

Position Summary:

The Senior 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. In this role, you will support the team in analyzing literature citations for individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of our customer’s products.

Duties and Responsibilities:

  • Critically analyze large numbers of articles from biomedical published literature and internal drug safety alerts
  • Identify individual case safety reports (ICSRs) and other potential safety relevant information impacting the risk-benefit and/or safety profile of customer’s products
  • Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article
  • Demonstrate understanding of client’s drugs labels and use that knowledge effectively in safety assessments
  • Complete drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner
  • Track all actions and assessments in an audit-ready reference history using our drug safety system
  • Select articles specific to client’s interest for inclusion in client’s product literature database
  • Write accurate, detailed, and complete abstracts of selected articles
  • Extract key points of articles and create comprehensive and detailed indexes of the abstract contents
  • Ensure timely completion of indexing and abstracting of articles for assigned drugs
  • Maintain awareness of new drugs and therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature
  • Participate in other duties such as searches and terminology maintenance according to business needs

Educational Qualifications:

  • Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.)
  • A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage
  • At least 5-6 years of experience reviewing biomedical literature for adverse event reporting or equivalent combination of education and experience
  • Related experience in drug safety/pharmacovigilance is desirable
  • Strong analytic ability to analyze and summarize biomedical case reports, studies, or specific topics
  • At least 5 years of experience using writing skills to support the creation of succinct, accurate, and precise summaries
  • At least 5 years of working knowledge of biomedical terminology, drugs, and therapeutic areas
  • Proficient in database/literature searches

Ancillary Qualifications:

The following qualifications are not necessarily required for this position, but they provide additional depth and value to the role:

  • Certification from a professional medical writer’s association
  • Experience with commercial and client-specific biomedical literature databases
  • Scientific/medical writing background


  • Excellent interpersonal, verbal, and written communication skills
  • Ability to work collaboratively and effectively in a team environment
  • Client-focused approach to work
  • Ability to evaluate data and draw conclusions independently
  • Ability to manage multiple and varied tasks and prioritize workload with attention to detail


Keywords: Clarivate Pharmacovigilance Jobs, Pharmacy, Senior Pharmacovigilance Specialist, Biomedical Literature, Adverse Events Reporting, Safety Assessments, Drug Safety, Pharmacovigilance Regulations. Clarivate Pharmacovigilance Jobs For Pharmacy – Apply Online. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.


Please enter your comment!
Please enter your name here