Alira Health
Alira Health is a global consulting firm that partners with life sciences companies to develop innovative solutions in healthcare. The company specializes in a wide range of services including research and clinical development, regulatory compliance, and management consulting. Alira Health focuses on patient engagement, market access, and providing real-world solutions to improve patient outcomes. They are committed to environmental sustainability and actively participate in community involvement and ESG initiatives. Alira Health also provides technology solutions with a focus on improving life sciences research through empathy and scientific excellence.
Nuclear medicine • Rare disease • Lupus • Myasthenia gravis • Robotics
Senior Clinical Research Associate
March 4
Alira Health
Alira Health is a global consulting firm that partners with life sciences companies to develop innovative solutions in healthcare. The company specializes in a wide range of services including research and clinical development, regulatory compliance, and management consulting. Alira Health focuses on patient engagement, market access, and providing real-world solutions to improve patient outcomes. They are committed to environmental sustainability and actively participate in community involvement and ESG initiatives. Alira Health also provides technology solutions with a focus on improving life sciences research through empathy and scientific excellence.
Nuclear medicine • Rare disease • Lupus • Myasthenia gravis • Robotics
📋 Description
• The Sr CRA is an important member of the Alira Health Clinical team. • The S r CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials. • Provides oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. • Works closely with US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance.
🎯 Requirements
• US: BS/BA from an undergraduate program (life sciences or related discipline preferred) • US: 3 years of experience in the pharmaceutical/biotechnology/CRO industry, 2 year of clinical monitoring experience with 1 year of management experience • EU: Minimum 2 years of clinical monitoring experience in the pharmaceutical/biotechnology/CRO industry and ability to autonomously manage monitoring activities • US: Permanent authorization to work in the U.S. • EU (Italy): Certified Monitor in compliance with Italian CRO decree dated 15Nov2011 • EU: Graduation in a scientific health field • Strong command of English, both written and verbal
🏖️ Benefits
• professional development • global travel • flexible work programs
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