Opportunity to work as Pharmacovigilance Specialist at Clarivate – Apply before 30th August 2024

About Clarivate

Clarivate is a global leader dedicated to accelerating innovation by providing comprehensive solutions that help customers solve some of the world’s most challenging problems. We deliver actionable insights and information to streamline the journey from novel ideas to groundbreaking inventions, particularly in the realms of science and intellectual property. Our expertise lies in helping clients discover, protect, and commercialize their innovations using trusted subscription services, technology-based solutions, and deep domain knowledge.

Job Title: Pharmacovigilance Specialist

Key Responsibilities

• Conduct structured searches of scientific literature databases (PubMed, Embase, etc.) using predefined strategies and keywords to identify safety information such as adverse events, safety signals, and emerging risks for assigned products.
• Perform secondary evaluations of references screened by primary screeners, ensuring accuracy before submission to the customer’s database.
• Index abstracts from relevant literature and work closely with the manager to provide constructive feedback to primary screeners, enhancing the quality of adverse event reporting.
• Stay informed about new pharmaceutical developments, therapeutic categories, emerging diseases, and changes in biomedical terminology to maintain the accuracy and relevance of the work.
• Extract pertinent safety data from selected literature sources, ensuring accuracy, completeness, and adherence to established protocols.
• Compile and organize extracted data clearly and systematically for further analysis and review.
• Collaborate with the Pharmacovigilance team to escalate potential safety signals and validate individual case safety reports (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.
• Ensure the accuracy and reliability of literature screening activities by adhering to standard operating procedures (SOPs) and quality control measures.
• Communicate literature screening findings and safety assessments effectively 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/Master’s degree in Pharmacy, Life Sciences, Nursing, or a related field. An advanced degree (e.g., PharmD, MD, PhD) is preferred.
• 2-3 years of experience in pharmacovigilance, medical literature analysis, or a related field within the pharmaceutical industry, with a focus on 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
• Application Deadline: 30th August 2024

Join Clarivate and contribute to a team that drives innovation and ensures safety in healthcare through cutting-edge research and data analysis.