Clinical Trial Manager (Retina)

Location: Remote within the United States; travel to clinical sites, conferences, and industry meetings as needed, approximately 5%.

Salary: $150,000–$170,000 base salary per year, with the final offer depending on geographic location, experience, skills, and years of experience.

Company

hirify.global is a late-stage biotechnology company developing durable, disease-targeted genetic medicines, including retinal and pulmonary therapies.

What you will do

• Manage day-to-day operations of one or more Phase 1–3 clinical trials across start-up, conduct, and close-out.
• Oversee CROs, monitors, service providers, consultants, investigational sites, and study deliverables.
• Lead cross-functional study execution, milestone tracking, metric reporting, issue resolution, and process improvement.
• Prepare and review clinical trial documentation, establish and maintain the Trial Master File, and keep records audit-ready.
• Manage study budgets, forecasts, invoices, site contracts, supplies, monitoring activities, data review, and protocol deviations.
• Support operational feasibility, site selection, staff training, audits, and clinical site visits.

Requirements

• B.A. or B.S. degree in Science.
• 6+ years of clinical research experience in biotechnology or a similar industry, including at least 2 years directly supporting a retina clinical trial.
• Knowledge of GCP, ICH guidelines, regulatory requirements, and clinical study management.
• Experience with protocol execution, site monitoring, risk mitigation, trial budgets, site selection, clinical supplies, and cross-functional collaboration.
• Strong communication, organization, negotiation, conflict-resolution, prioritization, problem-solving, and judgment skills.
• Proficiency with Microsoft Office Suite and working knowledge of MS Project for clinical study timelines.

Nice to have

• Global APAC clinical research experience.
• Experience overseeing or managing junior Clinical Operations staff.
• Experience developing or reviewing clinical SOPs.

Culture & Benefits

• Remote work arrangement within the United States.
• Opportunities to build therapeutic-area expertise through internal training and external conferences.
• Collaboration with cross-functional teams, external partners, CROs, and clinical sites.
• Sedentary office-based working conditions with occasional travel.