Clinical Study Manager

Alignerr Corp.; Portugal; Teletrabalho; EUR 55 000 - 96 000; Tempo integral

Resumo da oferta

Alignerr seeks an experienced Clinical Study Manager to shape how AI understands clinical research data, bringing rigorous trial operations, budgets, and vendor management to AI training. This is a fully remote hourly contract role.

You will evaluate, annotate, and improve AI outputs based on real-world study workflows and milestones, ensuring accuracy and regulatory alignment. Join a flexible, freelance-friendly environment with potential for ongoing projects across international sites and

Qualificações

• Extensive experience managing clinical trials and study operations.
• Ability to evaluate AI outputs against real-world trial standards.
• Strong documentation and feedback-writing skills.

Responsabilidades

• Oversee AI-generated clinical trial content for timelines, budgets, and vendor management.
• Assess accuracy, completeness, and quality of AI outputs.
• Review trial workflows and milestones for AI training datasets.
• Provide structured feedback to improve AI performance.
• Coordinate across multiple workstreams to meet deadlines.
• Work independently with flexible, asynchronous scheduling.

Conhecimentos

Clinical trial mgmt

Study operations

Vendor management

Ferramentas

EDC platforms

Descrição da oferta de emprego

What if your clinical trial management expertise could directly shape how AI understands and reasons about one of the most complex, high-stakes fields in the world? We're looking for experienced Clinical Study Managers to help build and validate AI systems trained on real-world clinical research data — bringing rigor, precision, and operational know-how to the frontier of AI development.

Clinical Study Manager (AI Training)

What if your clinical trial management expertise could directly shape how AI understands and reasons about one of the most complex, high-stakes fields in the world? We're looking for experienced Clinical Study Managers to help build and validate AI systems trained on real-world clinical research data — bringing rigor, precision, and operational know-how to the frontier of AI development.

This is a fully remote, flexible contract role. You'll apply your deep knowledge of clinical trial operations to evaluate, annotate, and improve AI outputs — helping ensure these models reflect the standards and realities of professional clinical research.

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

What You’ll Do

• Oversee and evaluate AI‑generated content related to clinical trial operations, timelines, budgets, and vendor management
• Apply your real‑world clinical research expertise to assess the accuracy, completeness, and quality of AI outputs
• Manage and review simulated or real clinical trial workflows, milestones, and deliverables as part of AI training datasets
• Identify gaps, errors, and inconsistencies in AI‑generated clinical research content and provide structured, detailed feedback
• Coordinate across multiple workstreams to ensure study‑related AI tasks are completed on time and to a high standard
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Experienced clinical trial professional with a strong background in study operations and project management
• Skilled at managing budgets, timelines, and vendor or CRO relationships across complex, multi‑site studies
• Naturally detail‑oriented with a systematic approach to identifying risks and resolving operational issues
• Clear and confident written communicator who can document findings precisely
• Self‑motivated and reliable when working independently without close supervision

Nice to Have

• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Familiarity with eClinical systems, EDC platforms, or clinical data management tools
• Background in regulatory affairs, GCP compliance, or clinical operations leadership
• Experience working across therapeutic areas or international multi‑site trials

Why Join Us

• Work on cutting‑edge AI projects alongside leading AI research labs and healthcare innovators
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, high‑impact work
• Gain exposure to advanced large language models (LLMs) and how they're trained using real‑world clinical expertise
• Contribute to AI development that has a genuine impact on the future of healthcare and clinical research
• Potential for ongoing work and contract extension as new projects launch