
11 - 50 employees
Founded 2018
🧬 Biotechnology
💊 Pharmaceuticals
🔥 Funding within the last year
💰 $402M Post-IPO Equity on 2025-12
Biotechnology • Pharmaceuticals
Belite Bio is a clinical-stage biopharmaceutical company developing novel therapeutics based on its RBP4 (Retinol Binding Protein 4) intellectual property portfolio. Its lead candidate, tinlarebant (LBS-008), is an oral therapy designed to reduce toxic accumulations in the eye and is being developed for retinal degenerative diseases including autosomal recessive Stargardt disease (STGD1) and Geographic Atrophy (advanced dry age-related macular degeneration). Belite Bio is conducting multiple clinical trials (Phase 1b/2, Phase 2/3, and Phase 3 programs such as DRAGON, DRAGON II, and PHOENIX) and tinlarebant has received several regulatory designations (Orphan Drug in US/EU/Japan, Rare Pediatric Disease, Breakthrough Therapy, Fast Track, and Sakigake). The company’s pipeline also includes programs addressing metabolic and liver diseases (e. g. , non-alcoholic fatty liver disease and type 2 diabetes).
🔥 2 minutes ago
Where this job comes from
Posted on Belite Bio's careers page, not through a job board
First seen by Remote Rocketship 2 minutes ago

11 - 50 employees
Founded 2018
🧬 Biotechnology
💊 Pharmaceuticals
🔥 Funding within the last year
💰 $402M Post-IPO Equity on 2025-12
Biotechnology • Pharmaceuticals
Belite Bio is a clinical-stage biopharmaceutical company developing novel therapeutics based on its RBP4 (Retinol Binding Protein 4) intellectual property portfolio. Its lead candidate, tinlarebant (LBS-008), is an oral therapy designed to reduce toxic accumulations in the eye and is being developed for retinal degenerative diseases including autosomal recessive Stargardt disease (STGD1) and Geographic Atrophy (advanced dry age-related macular degeneration). Belite Bio is conducting multiple clinical trials (Phase 1b/2, Phase 2/3, and Phase 3 programs such as DRAGON, DRAGON II, and PHOENIX) and tinlarebant has received several regulatory designations (Orphan Drug in US/EU/Japan, Rare Pediatric Disease, Breakthrough Therapy, Fast Track, and Sakigake). The company’s pipeline also includes programs addressing metabolic and liver diseases (e. g. , non-alcoholic fatty liver disease and type 2 diabetes).
• Lead Belite Bio’s technology infrastructure with a focus on quality assurance, regulatory compliance, and policy development • Ensure technology ecosystems are secure, scalable, and aligned with global compliance standards • Support IT asset management, including potentially configuring devices for new hires • Draft, implement, and maintain comprehensive IT policies, procedures, and standards • Maintain the IT Compliance policy and procedure inventory, including lifecycle tracking, review schedules, version control, approvals, publication, acknowledgments, retirement, and archival • Coordinate IT policy approval workflows with reviewers, approvers, Legal, Compliance leadership, and other stakeholders • Establish governance frameworks aligning IT strategy with business objectives and risk management protocols • Translate technical concepts and IT-related legal regulations into actionable internal policies • Oversee IT compliance with applicable regulations including GDPR, HIPAA, ISO 27001, FDA 21 CFR Part 11, and SOX • Lead internal and external IT audits and serve as primary contact for regulatory bodies and auditors • Conduct IT risk assessments and vulnerability analyses • Develop and enforce IT Quality Management Systems for software deployment, system validation, and infrastructure changes • Define and monitor KPIs and SLAs for IT quality • Provide vision and leadership for the IT department and manage technical professionals, engineers, and analysts • Manage the IT budget and optimize resources for hardware, software, vendor services, and compliance tooling • Collaborate with Legal, HR, and executive leadership on company-wide compliance goals
• Bachelor’s degree in Information Technology, Computer Science, Cybersecurity, or a related field • 8+ years of progressive IT experience • At least 3+ years in a leadership or directorial role • Proven track record of successfully writing, rolling out, and enforcing IT policies at an enterprise level • Deep experience managing IT compliance audits and working within structured quality frameworks • Exceptional technical writing skills • Strong understanding of modern IT infrastructure, cloud computing (AWS, Azure), network security, and data privacy laws • Excellent communication and interpersonal skills • Analytical mindset with strong problem-solving capabilities and high attention to detail • Certifications highly desired: CISA, CISM, CRISC, ITIL Foundation or Master certification, PMP
• Annual incentive bonuses • Equity participation • Health insurance • Dental insurance • Vision insurance • 401(k) • Paid time off
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