Are you passionate about drug safety and pharmacovigilance? We are looking for an Associate Pharmacovigilance Specialist to join our dynamic team in Karnataka, India! If you have a strong background in biomedical sciences and a keen eye for detail, we encourage you to apply.
About the Company
At Clarivate, we are dedicated to advancing the scientific and healthcare sectors through comprehensive insight and understanding. Our commitment extends to providing equal employment opportunities and creating an inclusive workplace. We focus on delivering data-driven solutions to our clients, ensuring the safety and efficacy of their products in line with regulatory standards. As part of our extensive team, you will be contributing to impactful projects that shape the future of healthcare.
Job Description
As an Associate Pharmacovigilance Specialist, you will play a crucial role in our pharmacovigilance services, focusing on biomedical literature monitoring to assess adverse events reporting. Your responsibilities will include:
- Analyzing biomedical literature and identifying individual case safety reports (ICSRs).
- Writing succinct narratives summarizing the ICSR criteria and any relevant safety information.
- Conducting drug safety reviews meticulously and in accordance with client standards.
- Utilizing drug safety systems to maintain a detailed, audit-ready reference history.
- Extracting key points from articles to create comprehensive abstracts and indexes.
- Keeping abreast of new drugs, therapeutic categories, and updates in biomedical terminology.
- Participating in additional duties as required based on business needs.
About You
To be successful in this role, you should possess:
- A Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, etc.).
- Preferably, a degree in Dentistry, Physiotherapy, or Nursing with hospital exposure.
- 1-2 years of experience in reviewing biomedical literature for adverse events reporting.
- Strong analytical skills to summarize case reports and studies.
- Proficient writing skills for creating accurate and precise summaries.
- Familiarity with biomedical terminology, drugs, and therapeutic areas.
- Excellent command of the English language, both written and verbal.
- Experience with commercial biomedical literature databases is advantageous.
- Certification from a professional medical writer’s association, while not mandatory, would be a plus.
Working Hours
This is a full-time permanent position with working hours Monday to Friday, from 11 AM to 8 PM IST.
How to Apply
