Alira Health
501 - 1000 employees
⚕️ Healthcare Insurance
💰 $58M Venture Round on 2023-01
Healthcare Insurance • Consulting
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.
Senior Clinical Research Associate
🕒 January 21
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Alira Health
501 - 1000 employees
⚕️ Healthcare Insurance
💰 $58M Venture Round on 2023-01
Healthcare Insurance • Consulting
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.
📋 Description
• Conduct site monitoring responsibilities for clinical trials • Provide oversight, leadership, and guidance in the management and execution of clinical trials • Ensure compliance and quality in clinical trial processes • Review monitoring visit reports and conduct co-monitoring and evaluation visits as required • Ensure appropriate and timely investigator site visits • Prepare consistent and timely monitoring visit reports documenting site-related problems and resolutions • Maintain regular contact with study sites to ensure protocol/GCP compliance
🎯 Requirements
• BS/BA from an undergraduate program (life sciences or related discipline preferred) • 3 years of experience in the pharmaceutical / biotechnology / CRO industry • 2 years of clinical monitoring experience with 1 year of management experience (US) • Minimum 2 years of clinical monitoring experience in the pharmaceutical / biotechnology / CRO industry (EU) • Ability to autonomously manage monitoring activities • Strong command of English, both written and verbal (US) • Strong command of Local language, both written and verbal, in the country where monitoring activities are performed (EU) • Certified Monitor in compliance with Italian CRO decree dated 15Nov2011 (EU)
🏖️ Benefits
• Professional development • Global travel • Flexible work programs
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