
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.
🕒 May 20
🍂 Massachusetts – Remote
💵 $55k - $70k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
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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.
• Manage and support clinical sites from site approval through close-out • Develop study documents and tools, including Informed Consent Form (ICF) templates • Support sites in obtaining IRB approval and developing submission materials • Respond to sites’ regulatory board requests for protocol and ICF clarification • Ensure all required site regulatory documents are in place prior to investigational product shipment • Conduct routine file reviews and analyze site performance problems • Maintain regular communication with study sites to ensure compliance • Conduct remote review of data entered on electronic Case Report Forms (eCRFs) • Assist with efforts to recruit investigative sites to participate in clinical studies • Comply with ICH GCP guidelines and FDA regulations • Participate in internal, client/sponsor, scientific, and other meetings as required • Manage and resolve conflicting priorities to deliver on commitments
• BS/BA from an undergraduate program or equivalent experience • 1-2 years of experience in clinical research • Proven ability to be careful, thorough, and detail-oriented • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment • Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills • Self-starter who thrives in a collaborative environment • Strong command of English, both written and verbal • Excellent communication and interpersonal skills with customer service orientation • Proficient with MS Office Suite, particularly Word and Excel • Permanent authorization to work in the U.S.
• Professional development • Global travel • Flexible work programs
Apply Now🕒 May 20
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