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.

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,  Click here

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.

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