Senior Pharmacovigilance Specialist vacancies in noida – Clarivate

Clarivate hiring Senior Pharmacovigilance Specialist
  • Full Time
  • Noida
  • 45000 INR / Month

Clarivate Careers: Hiring Senior Pharmacovigilance Specialist

Are You Passionate About Pharmacovigilance And Making A Positive Impact In Healthcare? Explore The Opportunity To Join Clarivate As A Senior Pharmacovigilance Specialist. Learn About The Role, Responsibilities, Qualifications, And How To Apply For This Rewarding Position.

About Clarivate: Clarivate Is A Global Leader In Providing Pharmacovigilance Services To Multiple Global Customers Across Therapeutic Areas. We Offer A Supportive Working Environment, Personalized Training, And Opportunities To Engage In Different Aspects Of Pharmacovigilance And Customer Engagement.

Job Overview: Senior Pharmacovigilance Specialist

  • Location: Noida, UP, India
  • Job Number: JREQ125692

Responsibilities:

  1. Biomedical Literature Monitoring: Critically Analyze Articles For Adverse Event Reporting And Identify Safety-Relevant Information Impacting Risk-Benefit Profiles.
  2. Narrative Writing: Write Concise And Accurate Summaries Of Individual Case Safety Reports (Icsrs) And Safety-Relevant Information.
  3. Drug Safety Review: Review Biomedical Literature Batches In Accordance With Client’s Standards And Regulatory Requirements.
  4. Indexing And Abstracting: Create Comprehensive Indexes And Abstracts Of Selected Articles For Precise Retrieval Of Literature.
  5. Timely Completion: Ensure Timely Completion Of Indexing, Abstracting, And Safety Assessments For Assigned Drugs.
  6. Continuous Learning: Stay Updated With New Drugs, Therapeutic Categories, And Changes In Biomedical Terminology.
  7. Team Collaboration: Work Collaboratively Within The Pharmacovigilance Team To Support Global Customers Across Therapeutic Areas.
Clarivate hiring Senior Pharmacovigilance Specialist
Clarivate hiring Senior Pharmacovigilance Specialist

Qualifications:

  • Education: Master’s Degree In Life Sciences, Health, Or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Etc.)
  • Experience: Minimum 5 Years Of Experience In Biomedical Literature Monitoring For Adverse Event Reporting Or Equivalent Combination Of Education And Experience.
  • Skills: Strong Writing Skills, Knowledge Of Biomedical Terminology, Drugs, And Therapeutic Areas, And Proficiency In MS Office Tools.

Work Environment:

  • Location: Noida, UP, India (Hybrid Work Mode Available)
  • Hours: 11:00 AM To 8:00 PM

Apply Now: Join Clarivate As A Senior Pharmacovigilance Specialist And Contribute To Impactful Work In Pharmacovigilance. Apply Today To Be Part Of Our Dedicated Team And Make A Difference In Healthcare Globally.

Accessibility Statement: Clarivate Is Committed To Providing Equal Employment Opportunities And A Supportive Work Environment For All. If You Require Accommodations During The Application Process, Please Contact Us For Assistance.

To apply for this job please visit careers.clarivate.com.

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