Clinical Study Manager

Alignerr Corp.; Charlotte (AR); Remote; USD 83,000 - 124,000; Part time

Job summary

Alignerr seeks an experienced Clinical Study Manager to oversee operational execution of clinical trials and contribute to AI systems trained on real‑world clinical data. This is a fully remote, hourly contract role for seasoned professionals managing timelines, budgets, and multi‑site coordination.

You will work with CROs, investigative sites, and internal teams to ensure quality and compliant study operations while supporting AI training initiatives in healthcare research.

Qualifications

• Experience managing budgets, timelines, and multi‑vendor coordination.
• Proven ability to manage CROs or external research partners and ensure deliverables.
• Strong communication skills to keep diverse stakeholders aligned and informed.
• Self‑driven, able to work autonomously in a remote, asynchronous environment.

Responsibilities

• Manage clinical trial timelines, milestones, and deliverables to keep studies on track and compliant with quality standards.
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and partners.
• Coordinate with CROs, investigative sites, and internal teams for smooth day‑to‑day operations in trials.
• Identify risks early, resolve operational issues, and keep stakeholders aligned throughout the lifecycle.
• Apply clinical expertise to inform AI systems being trained on healthcare data.

Skills

Budget management

Timeline management

Vendor coordination

CRO management

Risk assessment

Stakeholder communication

Remote work

Job description

About The Role

What if your clinical operations expertise could directly shape how AI understands and reasons about 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 AI systems that are being trained on real-world clinical data.

Clinical Study Manager (AI Training)

About The Role

What if your clinical operations expertise could directly shape how AI understands and reasons about 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 AI systems that are being trained on real-world clinical data.

This is a fully remote, flexible contract role built for seasoned clinical research professionals who know how to keep complex studies on track. If you've spent years wrangling timelines, vendors, and budgets across multi-site trials, this is a rare opportunity to apply that expertise at the intersection of clinical research and cutting-edge AI.

• 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 studies stay on track and meet quality standards
• Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners
• Coordinate with CROs, investigative sites, and internal teams to ensure smooth day-to-day study operations
• Identify risks early, resolve operational issues, and keep stakeholders aligned throughout the full trial lifecycle
• Apply your clinical expertise to evaluate and inform AI systems being trained on healthcare and research data

Who You Are

• Experienced clinical trial project manager with a strong track record across budgets, timelines, and multi-vendor coordination
• Confident managing CROs or external research partners and holding them accountable to deliverables
• Skilled at juggling multiple workstreams simultaneously without losing sight of quality or compliance
• A clear communicator who can keep complex stakeholder groups aligned and informed
• Self-motivated and comfortable working independently in a remote, asynchronous environment

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation workflows
• Familiarity with AI tools or platforms used in healthcare or clinical research settings
• Background in regulatory affairs, clinical data management, or trial monitoring

Why Join Us

• Work on cutting-edge AI and healthcare research projects alongside leading AI research labs
• Fully remote and flexible — structure your work around your life, not the other way around
• Freelance autonomy with the substance of meaningful, high-impact project work
• Gain direct exposure to advanced AI systems and how they're trained using real-world clinical data
• Potential for ongoing work and contract extension as new projects launch