Clinical Study Manager

Clinical Study Manager (AI Training) About The Role What if your clinical trial expertise could directly shape how AI understands and reasons about healthcare and medical research? We're looking for experienced Clinical Study Managers to help oversee the operational execution of clinical trials — and bring that real-world knowledge to some of the most advanced AI projects in the world. This is a fully remote, flexible contract role built for seasoned clinical operations professionals who want to do meaningful, high-impact work on their own schedule. 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 on budget Oversee study budgets, forecasting, and financial tracking across multiple vendors and research partners Coordinate with CROs, trial sites, and internal teams to ensure smooth, high-quality study execution Identify operational risks early, resolve issues decisively, and keep all stakeholders aligned throughout the trial lifecycle Apply your clinical research expertise to evaluate and improve AI-generated content in the healthcare and life sciences domain Who You Are Experienced clinical trial project manager with a strong track record of delivering complex studies on time and within budget Skilled at managing vendors, CROs, and external research partners across multiple concurrent workstreams Sharp operational thinker who can juggle competing priorities without losing attention to detail Clear, confident communicator — written and verbal — with the ability to align diverse stakeholders Self-directed and comfortable working independently in a remote, asynchronous environment Nice to Have Prior experience with data annotation, data quality review, or evaluation systems Familiarity with AI tools or healthcare AI applications Background in regulatory affairs, clinical data management, or medical writing Experience working across therapeutic areas or global multi-site trials Why Join Us Work on cutting-edge AI projects alongside the world's leading research labs Fully remote and flexible — work when and where it suits you Freelance autonomy with the structure of meaningful, high-value project work Gain direct exposure to advanced large language models trained on real-world clinical data Contribute to AI that could meaningfully shape the future of healthcare research Potential for ongoing work and contract extension as new projects launch

Manage clinical trial timelines, budgets, and vendor relationships to ensure high-quality study execution. Apply clinical research expertise to evaluate and improve AI-generated content within the healthcare and life sciences domain.

Requires extensive experience in clinical trial project management and a proven track record of delivering complex studies. Candidates should be skilled in managing external partners and comfortable working independently in a remote environment.

• Flexible schedule • Remote work • Freelance autonomy • Exposure to advanced large language models

• Gestion de projetSouhaitée
• CommunicationSouhaitée

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical trial management
• Project management
• Budgeting
• Forecasting
• Vendor management
• CRO coordination
• Risk management
• Stakeholder management
• Data annotation
• Data quality review
• Regulatory affairs
• Clinical data management
• Medical writing
• Communication
• AI evaluation

• Healthcare
• Science & Research
• Management & Leadership
• Technology
• Data & Analytics

Expérience minimale

5+ ans

Postuler avant le

11 sept. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Exigences de lieu

Country, Edmonton, Alberta, Canada

Niveau d’expérience

Mid-Senior level