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• Monitor and evaluate laboratory results daily from sponsor-designated central laboratories
• Conduct preliminary review of laboratory results relative to established protocol-specific reference range guidelines
• Evaluate laboratory data using clinical laboratory experience and compare current results with prior laboratory values
• Contact investigator sites for additional clinical information and distribute findings to the project team
• Serve as a liaison between the Medical Services Department, sponsor-designated laboratory, and IQVIA project team
• Identify significant trends or shifts in laboratory results and alert IQVIA Medical Advisors
• Facilitate appropriate monitoring and reporting of subject laboratory results with central laboratory staff
• Assist Lead Medical Surveillance Specialist with project setup activities
• Attend project team meetings as needed and perform other related duties as assigned
• Bachelor’s Degree in Life Sciences or allied health sciences (e.g., pharmacy, biochemistry, microbiology, biotechnology, nursing, medical laboratory sciences, physiotherapy, medical, or dentistry)
• 2 to 6 years of relevant experience with a minimum of 2.5 years in medical surveillance
• Strong technical ability to integrate scientific data from multiple sources
• Experience with word processing and data management
• Strong communication skills, both written and verbal
• Excellent organizational and analytical skills with attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Proficiency in computer skills and data management
• IQVIA is a global leader in providing clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. IQVIA accelerates the development and commercialization of medical treatments to improve patient outcomes and population health worldwide.