Clinical Study Manager

Alignerr Corp.; Portugal; Teletrabalho; EUR 34 000 - 62 000; Tempo integral

Resumo da oferta

Alignerr is seeking an experienced Clinical Study Manager to help build and validate AI systems trained on real-world clinical research data, bringing rigor, precision, and operational know-how to AI development. This is a fully remote, hourly contract role.

You will oversee AI-generated clinical content, manage study operations, timelines, budgets, and vendor relationships. We seek professionals with strong study operations backgrounds, attention to detail, and the ability to communicate

Qualificações

• Experienced clinical trial professional with strong study operations and PM experience.
• Skilled in budgets, timelines and vendor/CRO relationships across multi-site studies.
• Detail-oriented with a systematic approach to risk identification and issue resolution.
• Clear, confident written communicator documenting findings precisely.
• Self-motivated and reliable working independently.

Responsabilidades

• Oversee and evaluate AI-generated content on trial ops, timelines, budgets, and vendor management.
• Assess accuracy, completeness, and quality of AI outputs against real-world standards.
• Review trial workflows, milestones, and deliverables used for AI training.
• Identify gaps and provide structured feedback on AI-generated content.
• Coordinate across workstreams to ensure AI tasks meet deadlines and quality.
• Work independently and asynchronously on your own schedule.

Conhecimentos

Clinical trial mgmt

Budget management

Timeline management

Vendor management

CRO relationships

Ferramentas

EDC platforms

eClinical systems

Descrição da oferta de emprego

About The Role

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)

About The Role

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