Clinical Study Manager

Alignerr; 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

About The Role

What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — bringing real-world rigor to AI systems being trained on clinical data.

Clinical Study Manager (AI Training)

About The Role

What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare research? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — bringing real-world rigor to AI systems being trained on clinical data.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want to apply their expertise in a high-impact, forward-looking environment. If you've managed trials, wrangled vendor timelines, and kept complex studies on track, this role was designed for you.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 10–40 hours/week

What You'll Do

• 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

Who You Are

• 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

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation frameworks
• Familiarity with AI tools or clinical data platforms
• Background working on Phase I–III trials across therapeutic areas
• Experience with regulatory documentation and GCP compliance

Why Join Us

• Work at the intersection of clinical research and cutting-edge AI development alongside world-leading research labs
• Fully remote and flexible — structure your hours around your life, not the other way around
• Freelance autonomy with meaningful, substantive work that draws on your deepest expertise
• Gain exposure to how advanced AI models are trained using real-world clinical data — a genuinely rare venue
• Potential for ongoing work and contract extension as new projects launch