Associate Pharmacovigilance Specialist

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 - experience, education, skills, and accomplishments

• 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 1-2 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 analyze and summarize the main points of biomedical case reports, studies, or specific topics.
• At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries.
• At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas
• Excellent English language skills (comprehension, speaking, reading, and writing).
• Working knowledge of biomedical terminology, drugs, and therapeutic areas.
• Experience with commercial and client-specific biomedical literature databases.
• Basic computer literacy.

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

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.
• Selects articles specific to client s interest for inclusion in clients product literature database per guidelines.
• Writes accurate, detailed, and complete abstracts of selected articles using good judgement regarding the level of detail required and excellent organization, grammar, and syntax.
• Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from client s database.
• Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.
• Maintains an awareness of new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature.
• Participates in other duties such as searches and terminology maintenance according to business needs and per the training provided.

About the Team

The PV Literature team supports multiple customers covering all therapeutic areas. It is a supportive working environment with personalized training, and opportunities to engage in different aspects of pharmacovigilance and participate in customer upgrade planning if desired.

Hours of Work

This is a full-time permanent position working weekdays (Monday to Friday) , 11 am -8 PM IST

At Clarivate, we are committed to providing equal employment opportunities for all 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.