Alignerr logo

Clinical Study Manager

Alignerr
Department:Project Management
Type:REMOTE
Region:UK
Location:Christchurch, England, United Kingdom
Experience:Mid-Senior level
Estimated Salary:£60,000 - £90,000
Skills:
CLINICAL TRIAL MANAGEMENTBUDGET MANAGEMENTVENDOR MANAGEMENTCRO COORDINATIONRISK MANAGEMENTPROJECT MANAGEMENT
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Job Description

Posted on: May 8, 2026

Clinical Study Manager (AI Training)About The Role What if your clinical trial management expertise could directly shape how the world's most advanced AI understands healthcare and medical research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials that inform cutting-edge AI model development — ensuring studies run on time, within budget, and to the highest quality standards. This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want to contribute their expertise to projects at the frontier of AI and healthcare.

  • 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 projects on track and on schedule
  • Oversee study budgets, financial forecasting, and cost tracking across multiple vendors and research partners
  • Coordinate with CROs, investigative sites, and internal teams to ensure seamless operational execution
  • Proactively identify risks, resolve operational issues, and keep all stakeholders aligned throughout the full trial lifecycle
  • Apply your real-world clinical expertise to help train and evaluate AI systems that reason about medical research

Who You Are

  • Experienced clinical trial project manager with a strong track record of managing budgets, timelines, and complex deliverables
  • Skilled at managing external vendors, CROs, and research partners across multiple simultaneous workstreams
  • Highly organized, detail-oriented, and confident coordinating complex studies from kickoff through closeout
  • Clear communicator who can keep diverse teams aligned under pressure
  • 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 clinical data platforms
  • Background in regulatory affairs, clinical operations strategy, or medical writing

Why Join Us

  • Work on cutting-edge AI and healthcare research projects alongside leading research labs
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, high-impact project work
  • Gain rare exposure to advanced LLMs and how real-world clinical expertise shapes their development
  • Potential for ongoing work and contract extension as new projects launch
Originally posted on LinkedIn

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