Clinical Study Manager

Alignerr Corp.; Madrid; Remote; EUR 83,000 - 165,000; Part time

Job summary

Alignerr is seeking an experienced Clinical Study Manager (AI Training) to oversee operational execution of clinical trials and contribute to AI training datasets.

This fully remote hourly contract suits seasoned professionals who can manage timelines, budgets, CROs, and cross-functional teams while ensuring quality and regulatory alignment.

Qualifications

• Proven track record managing clinical trials in regulated environments.
• Experience with data annotation or AI datasets is a plus.
• Ability to work remotely and manage multiple workstreams.

Responsibilities

• Oversee trial timelines, milestones, and deliverables.
• Manage budgets and forecasts across vendors.
• Coordinate with CROs, sites, and internal teams.
• Identify risks and maintain stakeholder alignment.
• Contribute clinical insights to AI training datasets.

Skills

Clinical PM

Budget management

Vendor coordination

Stakeholder comms

Multi-site oversight

Job description

About The Role

What if your clinical trial expertise could directly shape how AI understands and supports the future of healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and in doing so, contribute to training the AI systems that will transform how medical research is conducted at scale.

Clinical Study Manager (AI Training)

About The Role

What if your clinical trial expertise could directly shape how AI understands and supports the future of healthcare research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and in doing so, contribute to training the AI systems that will transform how medical research is conducted at scale.

This is a fully remote, flexible contract role built for seasoned clinical operations professionals who thrive on keeping complex studies on track.

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

What You'll Do

• Manage clinical trial timelines, milestones, and deliverables to keep studies progressing on schedule
• Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and external partners
• Coordinate with CROs, investigative sites, and internal teams to ensure seamless study execution
• Identify operational risks early, resolve issues proactively, and maintain clear stakeholder alignment throughout the trial lifecycle
• Apply your real-world clinical expertise to inform and improve AI training datasets and evaluation frameworks

Who You Are

• Experienced in clinical trial project management, with a strong command of budgets, timelines, and deliverables
• Skilled at managing CROs, vendors, or external research partners in a regulated environment
• Comfortable juggling multiple concurrent workstreams without losing focus or quality
• A clear communicator who can align diverse stakeholders across complex, multi-site studies
• Self-directed and dependable when working remotely and independently

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation systems
• Familiarity with AI tools or research data workflows
• Background in early-phase, oncology, or multi-regional clinical trials

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
• Freelance autonomy with the variety and substance of meaningful, expert-level work
• Contribute directly to AI systems that will shape the future of healthcare and medical research
• Potential for ongoing work and contract extension as new projects launch