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, and therapeutic areas.
• Experience with commercial and client-specific biomedical literature databases.

It would be great if you also had . . .  

• Effective time management skills
• Excellent English written and verbal communication skills
• High motivation with a strong work ethic and ability to thrive in a fast-paced environment
• Adherence to SOP and Policies

What will you be doing in this role?

• Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures.
• Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article.
• Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.
• Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with client’s standards of timeliness and quality.
• Uses drug safety system to track all actions and assessments in an audit-ready reference history.

About Team:

Pharmacovigilance team at Clarivate provides services to multiple global customers covering all therapeutic areas. It provides a supportive working environment with personalized training, and opportunities to engage in different aspects of pharmacovigilance and customer engagement

      Hours of Work 

The team is based out of India (Bangalore or Noida ) and works 9:am IST to 6:00PM IST OR    11:00 AM to 8:00 PM (Mon-Friday) with Hybrid work mode

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.