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
🔥 14 minutes ago
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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
• The Sr 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 the Director of Clinical Monitoring and other CRAs. • Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues. • Prepares accurate monitoring visit reports documenting site-related problems.
🎯 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 years 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: Strong command of English, both written and verbal • EU: Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
🏖️ Benefits
• professional development • global travel • flexible work programs
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