Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida - PHARMA STUFF

SEND YOUR RESUME BELOW

Jun 25, 2024

Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida

associate-pharmacovigilance-specialist-vacancies-in-noida Associate Pharmacovigilance Specialist Vacancies in Noida - Your Gateway to a Rewarding Career Are you a skilled professional in the field of Life Sciences or Biomedical Sciences? Are you passionate about drug safety and ensuring the well-being of patients? Look no further – our client, Clarivate, is seeking talented individuals to join their dynamic team as Associate Pharmacovigilance Specialists in Noida. Dive into a fulfilling role where your expertise in biomedical literature monitoring and adverse event reporting will make a significant impact. About Clarivate: Clarivate is a global leader in providing pharmacovigilance services across various therapeutic areas. Committed to excellence, Clarivate offers a supportive working environment with personalized training and diverse opportunities for professional growth. Join a team dedicated to maintaining the highest standards of drug safety and customer engagement. Company Vacancies: Explore the exciting career opportunities at Clarivate. Here's a snapshot of the available positions:
  • Position Title: Associate Pharmacovigilance Specialist
  • Company Name: Clarivate
  • Salary: Competitive
  • Company Address: Noida, UP
  • Detailed Job Description: (Detailed job description provided below)
  • Role: Drug Safety
  • Industry Type: Pharma
  • Department: Pharmacovigilance
  • Employment Type: Full Time
  • Role Category: Medical/Healthcare
  • Educational Background Required: Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
  • Key Skills: Biomedical Literature Monitoring, Adverse Event Reporting, Writing Skills
Job Description: In this role, you will critically analyze biomedical literature, identify individual case safety reports (ICSRs), and contribute to the risk-benefit assessment of customer products. Your responsibilities include:
  • Summarizing ICSR criteria and safety-relevant information.
  • Utilizing drug safety systems for efficient tracking.
  • Reviewing and abstracting biomedical literature batches.
  • Writing accurate and detailed abstracts of selected articles.
  • Indexing articles for the client's product literature database.
  • Ensuring timely completion of indexing and abstracting.
About the Department & Responsibilities: Join the pharmacovigilance team at Clarivate, providing services across therapeutic areas. Engage in a supportive working environment, receive personalized training, and contribute to various aspects of pharmacovigilance and customer engagement. How to Apply: Ready to embark on this exciting career journey? Visit our careers page to apply for the Associate Pharmacovigilance Specialist position in Noida. Hours of Work: The team operates from 11:00 AM IST to 8:00 PM IST Monday-Friday, with a hybrid work mode. Candidates are required to work from the office at least 2 to 3 days a week. Important Information:
  • Company Name: Clarivate
  • Fraud Warning: Please be advised that recently there have been fraudulent job offers and interviews using the Clarivate name, logo, and even names of our colleagues.
[caption id="attachment_58522" align="aligncenter" width="1200"]associate-pharmacovigilance-specialist-vacancies-in-noida Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida[/caption] https://pharmastuff.org.in/job/associate-pharmacovigilance-specialist-noida-careers