
51 - 200 employees
Founded 2022
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
💰 $120M Venture Round - Aurion Biotechnologies on 2022-04
Healthcare • Manufacturing • Biotechnology
Aurion Biotech is a clinical-stage company developing first-in-class regenerative cell therapies to restore vision by treating corneal endothelial disease and other causes of blindness. The company focuses on manufacturing-scale cell therapy platforms, using human donor corneal endothelial cells combined with supportive compounds (e. g. , rho-kinase inhibitor) to repopulate the corneal endothelium, reduce reliance on donor tissue, and enable less-invasive alternatives to graft-based keratoplasty. Aurion conducts global clinical trials, holds FDA Breakthrough Therapy and RMAT designations for its lead product AURN001, and aims to expand access to advanced ophthalmic care worldwide.
🔥 1 minute ago
🐎 Kentucky, New Hampshire, +12 more states – Remote
💵 $92k - $120k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Aurion Biotech's careers page, not through a job board
First seen by Remote Rocketship 1 minute ago
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51 - 200 employees
Founded 2022
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
💰 $120M Venture Round - Aurion Biotechnologies on 2022-04
Healthcare • Manufacturing • Biotechnology
Aurion Biotech is a clinical-stage company developing first-in-class regenerative cell therapies to restore vision by treating corneal endothelial disease and other causes of blindness. The company focuses on manufacturing-scale cell therapy platforms, using human donor corneal endothelial cells combined with supportive compounds (e. g. , rho-kinase inhibitor) to repopulate the corneal endothelium, reduce reliance on donor tissue, and enable less-invasive alternatives to graft-based keratoplasty. Aurion conducts global clinical trials, holds FDA Breakthrough Therapy and RMAT designations for its lead product AURN001, and aims to expand access to advanced ophthalmic care worldwide.
• Support the clinical development team with scientific and medical oversight throughout study startup, enrollment, conduct, database lock, and study closeout • Support Medical Monitoring activities and patient cleaning activities, including medical monitor query management • Identify clinical risks and help develop mitigation strategies • Support development of study protocols, protocol amendments, informed consent documents, case report forms, and other clinical study documents • Help address protocol questions, eligibility determinations, deviations, and study conduct challenges • Ensure clinical studies comply with protocol requirements, ICH-GCP, applicable regulations, and Aurion SOPs • Partner with Biometrics and/or Data Management to develop data review plans and ensure data quality • Review clinical, efficacy, safety, imaging, and biomarker/pharmacokinetic data • Contribute to regulatory meeting preparation and interactions with global health authorities • Support briefing documents, responses to agency questions, and submission documents • Contribute scientific content for INDs, CTAs, annual reports, clinical study reports, and marketing applications • Collaborate with Clinical Operations, Medical Affairs, Regulatory Affairs, Biometrics, Pharmacovigilance, Quality Assurance, CRO partners, imaging centers, and other vendors • Support inspection readiness activities and participate in audits and regulatory inspections • Contribute to continuous process improvement initiatives within Clinical Development • Support a collaborative, high-performance culture aligned with Aurion Biotech’s mission and values
• Strong background in ophthalmology, ophthalmology clinical trials, and interpretation of ophthalmology data including visual acuity procedures and image collection • Bachelor’s degree in life sciences, nursing, or related field preferred • 1-3 years of experience in clinical research, including exposure to clinical trial operations, either in a sponsor, CRO, or academic setting supporting Phase 2 or 3 clinical trials • Familiarity with study start-up, site maintenance, closeout, and inspection readiness processes • Working knowledge of ICH/GCP guidelines and clinical trial processes • Strong organizational and time management skills; detail-oriented and able to manage multiple tasks • Proficient in Microsoft Office (Word, Excel, PowerPoint) • Experience with TMF, EDC, and other clinical trial systems a plus • Strong interpersonal and communication skills, both written and verbal • Ability to work effectively in a team environment and across global teams and vendors • Excellent written, verbal, and interpersonal communication skills; ability to communicate with impact across diverse internal and external stakeholders • Demonstrated cultural agility, integrity, and a passion for advancing transformative science • Ability to travel up to 15% • Strong alignment with, and commitment to, Aurion Biotech’s mission, vision, and core values
• Full health insurance for employees and their families • 401(k) matching • EAP • FSA • Generous PTO • Paid parking • Subsidized commuter passes • In-office catered lunches • Team events • Community projects • Competitive compensation packages
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