Senior Pharmacovigilance Specialist vacancies in noida – Clarivate

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: JREQ129642

Responsibilities:

• Develop and refine literature search strategies and methodologies to ensure comprehensive and systematic screening of scientific literature databases, including MEDLINE/PubMed, Embase, Biosis Previews, and other biomedical databases. Proficient in searching literature for NDA, PSUR, DSUR, AER, and client-requested searches to identify relevant safety information, including adverse events, safety signals, and emerging risks associated with assigned products.
• Supports the development and execution of a literature search training program that aligns with internal guidelines, industry best practices, and is flexible enough to include customer-specific directives. Helps the leads and Managers in the internal training of new recruits and organizes regular refresher training sessions for the entire team. Assesses the performance of trainees, keeps training records up-to-date, and ensures documentation is ready for audits.
• Analyses search requests from clients and designs and inputs search strategies that result in specific and accurate retrieval from commercial databases.
• Maintains an awareness of new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature to provide for continuing responsiveness to department databases.
• Participates in assignment tracking, client communications, and reporting, as requested.
• Holds good knowledge of biomedical searching platforms such as Dialog, PubMed, or related platforms and understands how to apply thesauri such as MeSH and Emtree.
• Aids in addressing system-related issues of the hierarchies and their application in retrieval strategies.
• Co-operates with retrieval and abstract/index specialists on term assignments to confirm the appropriateness of solutions and instigates discussions of varying perspectives to ensure adherence to best practices.
• Establishes effective collaborations with customers during the pre-and post-sales process to comprehend specific procedures and receive training tailored to the customer’s needs.

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 Online By Click here

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.

Tagged as: Good Clinical Practice (GCP), Pharmacology