
501 - 1000 employees
🏥 Healthcare
🏭 Manufacturing
⚕️ Healthcare Insurance
💰 $58M Venture Round on 2023-01
Healthcare • Manufacturing • Healthcare Insurance
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.
🕒 July 2
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501 - 1000 employees
🏥 Healthcare
🏭 Manufacturing
⚕️ Healthcare Insurance
💰 $58M Venture Round on 2023-01
Healthcare • Manufacturing • Healthcare Insurance
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.
• 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.
• 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
• professional development • global travel • flexible work programs
Apply Now🕒 June 5
Clinical Scientist Associate Director at Amgen supporting design, execution, and oversight of global clinical trials. Collaborating with cross-functional teams to deliver high-quality clinical data for regulatory submissions and scientific dissemination.
🇪🇸 Spain – Remote
💵 €90.8k - €122.8k / year
💰 $28.5G Post-IPO Debt on 2022-12
⏰ Full Time
🟠 Senior
🧪 Clinical Research
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