Clinical Trial Manager

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $128k - $150k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Character Biosciences

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2019

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

🔥 Funding within the last year

💰 $17M Series B - Character Biosciences on 2025-09

Healthcare • Consulting • Biotechnology

Character Biosciences is a precision medicine biotechnology company focused on understanding and treating progressive polygenic eye diseases, with an initial emphasis on age-related macular degeneration (AMD) and primary open-angle glaucoma (POAG). The company integrates large human genomic datasets with longitudinal clinical data, retinal imaging, and AI-enabled biomarker quantification to identify genetic drivers of disease progression and to guide targeted drug discovery and development. Character Biosciences partners with healthcare providers, patients, and industry collaborators to translate genomic and machine-learning insights into more effective, subtype-targeted ophthalmology therapies.

📋 Description

• Own day-to-day operational delivery of one or more clinical trials from startup through close-out • Drive study timelines, quality, and issue resolution • Develop and maintain study timelines, clinical plans, risk mitigation plans, and operational trackers • Escalate issues before they affect delivery • Manage CROs, central labs, imaging vendors, and site performance • Hold vendors accountable to scope, quality, and timelines • Track enrollment, monitoring visit completion, and data quality metrics • Drive corrective action where needed • Ensure studies comply with GCP, the protocol, and applicable regulations • Maintain trial master file completeness and inspection readiness • Track study-level spend against budget • Flag budget variances and support invoice and payment review • Partner with cross-functional stakeholders to align study execution with program strategy • Provide timely updates on study status, risks, and timelines to program leadership

🎯 Requirements

• Typically 3-5 years of Clinical Operations experience, including hands-on study startup, vendor oversight, and compliance management • Bachelor’s degree required; advanced degree helpful but not required • Strong command of clinical trial execution across study phases • Ophthalmology or retina experience strongly preferred • Proven experience managing CROs, vendors, and sites • Solid understanding of GCP and clinical trial regulations • Regulatory agency inspection experience preferred • Ability to lead cross-functional study teams and interface directly with external vendors and sites • Strong organizational and communication skills • Ability to balance competing priorities across studies • High integrity and high reliability • Comfort operating with a high degree of independence • Applicants must be authorized to work in the United States

🏖️ Benefits

• Equity • Medical insurance • Dental insurance • Vision insurance • 401(k) • Accrued paid time off policy • Competitive salary • Strong equity incentives • Diversity, equity, and inclusion commitment