Pharmacovigilance Jobs: Clarivate is Hiring Associate Pharmacovigilance Specialist | Apply Now
Looking for trusted and growth-driven pharmacovigilance jobs? This Associate Pharmacovigilance Specialist role at Clarivate offers a strong entry point for professionals wanting to advance in drug safety, literature screening, and regulatory compliance. If you’re exploring Life science jobs that blend research, analysis, and global impact, this Clarivate career opportunity in Noida could be your pathway to a secure and rewarding future.
Job Details:
- Job Title: Associate Pharmacovigilance Specialist – Literature Screening
- Location: Noida, Uttar Pradesh, India
- Work Model: Hybrid
About the Company:
Clarivate is a global leader in data-driven insights, analytics, and scientific information solutions. Known for its contributions to research, healthcare, and life sciences innovation, Clarivate supports organizations worldwide by delivering accurate, real-time intelligence that powers critical decisions.
With a strong focus on scientific integrity and innovation, Clarivate provides outstanding opportunities for professionals seeking meaningful pharmacovigilance jobs and long-term Clarivate career growth. Its commitment to workplace inclusivity, continuous learning, and cutting-edge research makes it a preferred choice for candidates across various Life science jobs domains.
Key Responsibilities:
- Evaluate literature reports for adverse events or safety concerns requiring escalation.
- Extract and document safety data from scientific publications with high accuracy.
- Enter relevant data into pharmacovigilance databases or tracking systems.
- Maintain organized documentation for all literature screening activities.
- Stay updated on evolving PV regulations and global safety requirements.
- Incorporate new knowledge into daily literature evaluation practices.
Education:
Bachelor’s degree or equivalent in Life Sciences, or related field with 1 Year of Relevant Experience
Skills Required:
- Strong understanding of pharmacovigilance principles
- Attention to detail and analytical thinking
- Ability to interpret scientific literature
- Familiarity with safety databases (preferred)
- Strong written communication skills
- Knowledge of regulatory guidelines and scientific terminology
This Clarivate career opportunity is ideal for individuals wanting to grow in the field of drug safety and literature screening. Whether you’re transitioning within Life science jobs or strengthening your expertise in PV, this position offers a stable, skill-enhancing pathway within a global organization committed to innovation, accuracy, and regulatory excellence.
