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:
- Biomedical Literature Monitoring: Critically Analyze Articles For Adverse Event Reporting And Identify Safety-Relevant Information Impacting Risk-Benefit Profiles.
- Narrative Writing: Write Concise And Accurate Summaries Of Individual Case Safety Reports (Icsrs) And Safety-Relevant Information.
- Drug Safety Review: Review Biomedical Literature Batches In Accordance With Client's Standards And Regulatory Requirements.
- Indexing And Abstracting: Create Comprehensive Indexes And Abstracts Of Selected Articles For Precise Retrieval Of Literature.
- Timely Completion: Ensure Timely Completion Of Indexing, Abstracting, And Safety Assessments For Assigned Drugs.
- Continuous Learning: Stay Updated With New Drugs, Therapeutic Categories, And Changes In Biomedical Terminology.
- Team Collaboration: Work Collaboratively Within The Pharmacovigilance Team To Support Global Customers Across Therapeutic Areas.
[caption id="attachment_70643" align="aligncenter" width="1200"]
Clarivate hiring Senior Pharmacovigilance Specialist[/caption]
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.
https://pharmastuff.org.in/job/clarivate-senior-pharmacovigilance-specialist?feed_id=9753
