Clarivate, where innovation meets expertise. We are thrilled to announce opportunities for talented individuals to join us as Pharmacovigilance Specialists in Noida. If you have a passion for healthcare and the skills to make a difference, Clarivate is the place for you.
About Clarivate
Company Overview:
- Name: Clarivate Analytics
- Location: Noida, UP
- City, ST: Noida, UP
Clarivate Vacancies List
Discover your potential as a Pharmacovigilance Specialist:
- Position: Pharmacovigilance Specialist
- Job Number: JREQ125697
- City, ST: Noida, UP
Job Description
Position: Pharmacovigilance Specialist
Reports To: Director, Consulting; Senior Manager, Pharmacovigilance; Manager, Pharmacovigilance
Organization: Clarivate Analytics
Position Summary:
As a Pharmacovigilance Specialist, you will perform essential pharmacovigilance services, including biomedical literature monitoring, adverse events reporting, indexing, and abstracting. Your role demands a broad understanding of scientific terms, medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Duties and Responsibilities:
- Critically analyze biomedical literature and internal drug safety alerts.
- Identify individual case safety reports (ICSRs) and safety-relevant information.
- Write brief narratives summarizing ICSR criteria and safety-relevant information.
- Demonstrate understanding of client’s drugs labels for effective safety assessments.
- Complete drug safety reviewing in a timely, thorough, and accurate manner.
- Use drug safety systems for audit-ready reference history tracking.
- Write accurate abstracts of selected articles with excellent organization and syntax.
- Extract key points of articles and create comprehensive indexes of abstract contents.
- Ensure timely completion of indexing and abstracting for assigned drugs.
Educational Qualifications:
- Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
- A degree in Dentistry/physiotherapy/Nursing, with patient exposure, would be an advantage.
- 2-4 years of experience in reviewing biomedical literature for adverse event reporting.
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Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida[/caption]
Ancillary Qualifications:
While not mandatory, the following qualifications provide additional depth and value to the role:
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Scientific/medical writing background.
Skills:
- Excellent English language skills (comprehension, speaking, reading, and writing).
- Working knowledge of biomedical terminology, drugs, and therapeutic areas.
- Experience with commercial and client-specific biomedical literature databases.
- Flexibility and adaptability to changing client needs.
- Ability to work effectively, independently, and collaboratively.
- Basic computer literacy.
The preceding job description provides a general overview of expectations and responsibilities. As business demands change, additional duties may be assigned.
How to Apply
For detailed application procedures,
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At Clarivate, we are committed to providing equal employment opportunities for all. We comply with applicable laws and regulations governing non-discrimination in all locations.
Fraud Warning: Be aware of fraudulent job offers using the Clarivate name. Clarivate will never ask for payment or sensitive personal information during the hiring process.
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