
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.
November 13
🗣️🇳🇱 Dutch Required

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.
• Conduct site monitoring responsibilities for clinical trials, providing oversight, leadership, and guidance in management and execution • Ensure protocol compliance, address site questions, assist with recruitment, training and other site-related issues • Provide guidance and feedback to CRA team, review monitoring visit reports, conduct co-monitoring visits • Coordinate with cross-functional departments for clinical trial monitoring related issues • Prepare accurate and timely monitoring visit reports documenting site-related problems, resolutions, and study progress • Ensure integrity of CRF data and performs quality control of documents at sites
• 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 • 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.
• Professional development • Global travel • Flexible work programs
Apply NowNovember 5
Clinical Research Associate II/Senior CRA responsible for monitoring clinical studies at investigative sites for Precision for Medicine. Ensuring compliance with protocols, regulations, and clinical standards.
🇧🇪 Belgium – Remote
đź’° $75M Private Equity Round on 2015-12
⏰ Full Time
đźź Senior
🔬 Research Analyst
🗣️🇫🇷 French Required
🗣️🇳🇱 Dutch Required
November 5
1001 - 5000
🧬 Biotechnology
⚕️ Healthcare Insurance
đź’Š Pharmaceuticals
Clinical Research Associate II/Senior CRA monitoring and managing clinical studies remotely for a global CRO. Ensuring compliance with regulations and mentoring junior staff in Belgium.
🇧🇪 Belgium – Remote
đź’° $35.2M Venture Round on 2021-03
⏰ Full Time
đźź Senior
🔬 Research Analyst
🗣️🇫🇷 French Required
🗣️🇳🇱 Dutch Required