Remote Clinical Study Manager for AI Training

Alignerr Corp.; France; Remote; EUR 48,000 - 90,000; Part time

Job summary

Alignerr is seeking a Clinical Study Manager to oversee operational execution of clinical research projects for AI training. This fully remote, hourly contract role is designed for seasoned clinical operations professionals who want to apply their expertise in a high-impact, forward-looking environment.

If you've managed trials, coordinated CROs and vendors, and kept complex studies on track, this role offers freelance autonomy with meaningful, substantive work and potential for ongoing

Qualifications

• Experienced clinical trial project manager with a strong track record managing budgets, timelines, and multi-vendor studies.
• Skilled at coordinating CROs, external research partners, and cross-functional internal teams.
• Comfortable managing multiple workstreams simultaneously without letting anything fall through the cracks.
• Detail-oriented and proactive — you spot problems before they become crises.
• Clear, structured communicator who keeps everyone aligned in complex, fast-moving environments.

Responsibilities

• Manage clinical trial timelines, milestones, and deliverables to ensure projects stay on track and within scope.
• Oversee study budgets, financial forecasting, and expenditure tracking across multiple vendors and research partners.
• Coordinate with CROs, investigative sites, and internal teams to ensure smooth, high-quality study execution.
• Identify operational risks early, resolve issues proactively, and keep stakeholders aligned throughout the trial lifecycle.
• Apply your clinical research expertise to support AI training projects grounded in real-world study data.

Job description

Alignerr is seeking a Clinical Study Manager to oversee operational execution of clinical research projects for AI training. This fully remote, hourly contract role is designed for seasoned clinical operations professionals who want to apply their expertise in a high-impact, forward-looking environment.

If you've managed trials, coordinated CROs and vendors, and kept complex studies on track, this role offers freelance autonomy with meaningful, substantive work and potential for ongoing