
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.
🔥 0 minutes ago
🐎 Kentucky, New Hampshire, +10 more states – Remote
💵 $95k - $113k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🦅 H1B Visa Sponsor
Improve your chances of getting an interview by checking your resume score before you apply.

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 clinical trial teams with operational aspects of studies across start-up, conduct, and close-out for insourced and outsourced trials • Support procurement activities, including vendor contracts and purchase orders • Support management of clinical supplies and clinical trial equipment provision and reclamation • Manage study-level documents in the Trial Master File (TMF) and support TMF audits • Generate reports from EDC, CTMS, and third-party vendor portals • Generate newsletters, newsblasts, checklists, and other site-level communications • Track and manage study data and metrics • Support data quality and site performance metrics, including query resolution and database lock readiness • Support inspection readiness activities, audits, audit report finalization, findings, and CAPAs • Collaborate with Clinical Operations, Regulatory, Quality, Medical, and CMC teams • Support Study Leads with vendor and system onboarding, training coordination, and process documentation • May support monitoring quality oversight and site engagement visits • Ensure compliance with GCP, ICH, Aurion SOPs, and CRO SOPs • Perform other duties as assigned
• Bachelor's degree in life sciences, nursing, or a related field • 2–4 years of experience in clinical research, including exposure to clinical trial operations in a sponsor, CRO, or academic setting • Experience 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 • Proficiency in Microsoft Office (Word, Excel, PowerPoint) • Experience with Canva, CTMS, TMF, EDC, and other clinical trial systems is a plus • Strong written, verbal, and interpersonal communication skills • Ability to work effectively in a team environment and across global teams and vendors • Demonstrated cultural agility and integrity, with passion for advancing transformative science • Ability to travel up to 15% • Commitment to Aurion Biotech's mission, vision, and core values • Candidates must be based in WA, MA, IN, NC, NJ, NH, NM, NY, PA, SC, SD, TX, or KY
• Full health insurance for employees and their families • 401(k) matching • Employee Assistance Program (EAP) • Flexible Spending Account (FSA) • Generous PTO • Paid parking • Subsidized commuter passes • In-office catered lunches • Team events • Community projects • Competitive compensation packages
Apply Now🔥 8 hours ago
Clinical Trial Manager overseeing clinical studies and regulatory deliverables for Thermo Fisher Scientific, a global science-services company. Managing monitoring, documentation, timelines, resources, and client coordination.
🔥 17 hours ago
Clinical Data Manager designing and validating trial databases for the American College of Radiology’s radiology research programs. Ensuring high-quality data from study startup through completion.
🇺🇸 United States – Remote
💵 $73k - $80k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 17 hours ago
Clinical Data Manager supporting radiology clinical research trials at the American College of Radiology. Designing, validating, and overseeing clinical trial databases and data collection systems.
🇺🇸 United States – Remote
💵 $73k - $80k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 21 hours ago
Clinical Research Associate II supporting AbbVie’s innovative medicines through clinical-site monitoring in Southern California. Managing site engagement, compliance, recruitment, data quality, and patient-safety risk across clinical trials.
🇺🇸 United States – Remote
💵 $84.5k - $162k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 21 hours ago
Remote Global Study Manager coordinating clinical research studies for Labcorp, a global laboratory services and life sciences company. Managing client delivery, budgets, risks, milestones, and stakeholder communications across central laboratory operations.
🇺🇸 United States – Remote
💵 $70k - $90k / year
💰 $2G Post-IPO Debt - LabCorp on 2024-09
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research