Remote Clinical Study Manager for AI Training

Alignerr Corp.; Cincinnati (OH); Remote; USD 83,000 - 165,000; Part time

Job summary

Alignerr is seeking an experienced Clinical Study Manager to shape AI-driven healthcare research. This fully remote, hourly contract role values real-world trial expertise to supervise timelines, budgets, vendors, and trial operations, ensuring quality and compliance in AI training data and workflows.

You will coordinate with CROs, clinical sites, and internal teams, manage risk, and continuously improve AI-generated content for clinical research while thriving in a flexible, asynchronous work

Qualifications

• Experienced in clinical trial project management, with a strong command of budgets, timelines, and milestone tracking.
• Proven track record managing vendors, CROs, or external research partners.
• Skilled at juggling multiple workstreams and keeping complex, multi-site studies running smoothly.

Responsibilities

• Manage clinical trial timelines, milestones, and deliverables to ensure studies stay on track and meet quality standards.
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners.
• Coordinate with CROs, clinical sites, and internal teams to support smooth execution of trial operations.
• Identify operational risks early, resolve issues proactively, and keep all stakeholders aligned throughout the trial lifecycle.
• Apply your clinical expertise to evaluate and improve AI-generated content and workflows related to clinical research.

Skills

Clinical trial management

Budgeting

Vendor management

Timeline tracking

Risk management

Cross-functional communication

Tools

AI tools

Clinical data platforms

Job description

Alignerr is seeking an experienced Clinical Study Manager to shape AI-driven healthcare research. This fully remote, hourly contract role values real-world trial expertise to supervise timelines, budgets, vendors, and trial operations, ensuring quality and compliance in AI training data and workflows.

You will coordinate with CROs, clinical sites, and internal teams, manage risk, and continuously improve AI-generated content for clinical research while thriving in a flexible, asynchronous work