Clarivate is a global leader in providing solutions to accelerate the lifecycle of innovation. The company helps customers solve complex problems by offering actionable information and insights that reduce the time from new ideas to life-changing inventions in science and intellectual property.

Job Overview

Position: Pharmacovigilance Specialist

Company Profile: Clarivate is committed to helping customers solve complex problems with actionable insights and information, making significant contributions to science and intellectual property.

Job Duties and Responsibilities

• Conduct structured searches of scientific literature databases (e.g., PubMed, Embase) using predefined search strategies and keywords.
• Screen search results to identify relevant safety information, including adverse events, safety signals, and emerging risks associated with assigned products.
• Conduct secondary evaluation of references screened and submitted by primary screeners.
• Index abstracts from literature and provide constructive feedback to primary screeners to enhance the quality of adverse event (AE) reporting.
• Stay updated on new pharmaceutical developments, therapeutic categories, emerging diseases, and modifications in biomedical terminology.
• Extract pertinent safety data from selected literature sources, ensuring accuracy and completeness.
• Compile and organize extracted data for further analysis and review.
• Collaborate with the Pharmacovigilance team to escalate potential safety signals and valid ICSRs for further evaluation and risk assessment.
• Evaluate literature reports for potential cases of adverse events or safety concerns requiring further investigation.
• Maintain detailed documentation of literature screening activities, including search strategies, screening criteria, and data extraction methods.
• Prepare concise summaries of literature findings and safety assessments for internal reporting purposes.
• Ensure accuracy and reliability of literature screening activities by adhering to standard operating procedures (SOPs) and quality control measures.
• Effectively communicate literature screening findings and safety assessments to internal stakeholders.
• Collaborate with cross-functional teams to provide timely updates on relevant safety information and contribute to risk management decisions.

Candidate Profile

• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, or a related field. Advanced degree (e.g., PharmD, MD, PhD) preferred.
• Previous 2-3 years of experience in pharmacovigilance, medical literature analysis, or a related field within the pharmaceutical industry, preferably with experience in literature screening.
• Strong understanding of pharmacovigilance principles, adverse event reporting requirements, and regulatory guidelines.
• Familiarity with scientific literature databases and search techniques (e.g., PubMed, Embase).

Additional Information

• Experience: 2-3 years
• Qualification: Bachelor’s/Master’s degree in Pharmacy, Life Sciences
• Location: Karnataka; Noida, Uttar Pradesh, India
• Functional Area: Life Sciences & Healthcare
• End Date: 30th August 2024

Interested candidates are encouraged to apply by the end date. If you have further questions or need assistance with the application process, feel free to ask!

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