Alira Health
501 - 1000 employees
âïž Healthcare Insurance
đ° $58M Venture Round on 2023-01
Healthcare Insurance âą 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
đ„ 14 minutes ago
đŁïžđ«đ· French Required
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Alira Health
501 - 1000 employees
âïž Healthcare Insurance
đ° $58M Venture Round on 2023-01
Healthcare Insurance âą 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.
đ Description
âą Conduct site monitoring responsibilities for clinical trials âą Provide oversight, leadership, and guidance in the management and execution of clinical trials âą Ensure protocol compliance and assist with study recruitment âą Review monitoring visit reports and ensure timely investigator site visits âą Maintain regular contact with study sites to ensure protocol/GCP compliance âą Participate in internal, client/sponsor, scientific, and other meetings as required
đŻ Requirements
âą US: BS/BA from an undergraduate program (life sciences or related discipline preferred) âą US: 3 years of experience in the pharmaceutical/biotechnology/CRO industry, 2 year of clinical monitoring experience with 1 year of management experience âą EU: Minimum 2 years of clinical monitoring experience in the pharmaceutical/biotechnology/CRO industry and ability to autonomously manage monitoring activities âą EU: Fluent in English and French âą Knowledge of clinical research, ICH GCP, and local regulations âą Strong command of English, both written and verbal âą Strong command of Local language, both written and verbal, in the country where monitoring activities are performed
đïž Benefits
âą Professional development âą Global travel âą Flexible work programs
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