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Alignerr

Clinical Study Manager

Alignerr

Remote ・ 契約

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2時間前
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在宅勤務
Eligibility
Experienced clinical operations or clinical trial professionals who can work remotely on a flexible hourly contract and contribute practical trial-management expertise to AI training work.
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仕事内容

About the role

This remote contract opportunity is designed for experienced clinical operations professionals who can bring practical trial-management knowledge into AI training work. The role centers on using real-world clinical study expertise to help AI systems better understand how healthcare research is planned and executed.

The work is flexible and suited to seasoned professionals who are comfortable handling study operations, maintaining control over timelines and budgets, and keeping trials inspection-ready.

Role details

  • Organization: Alignerr
  • Engagement type: Hourly contract
  • Work setup: Remote
  • Expected commitment: 10 to 40 hours per week

What you will do

  • Track study schedules, milestones, and deliverables so trials remain on course from start-up through closeout.
  • Monitor budgets, forecasts, and financial activity across vendors and research collaborators.
  • Work with CROs, site teams, and internal stakeholders to support compliant and efficient study execution.
  • Spot operational risks early, address problems proactively, and keep everyone aligned throughout the study lifecycle.
  • Use your clinical research experience to assess and improve AI-generated content related to study workflows.

What we are looking for

We are seeking a clinical trial professional with solid study project management experience, especially in budget oversight and timeline management. The ideal candidate has worked with vendors, CROs, and external research partners across more than one study at a time.

You should be comfortable managing multi-workstream projects, staying organized under pressure, and communicating clearly in writing. This role also calls for a self-directed professional who can work independently in a remote setting.

Preferred experience

  • Exposure to data annotation, data review, or evaluation workflows.
  • Familiarity with AI tools or content assessment processes.
  • Background in regulatory compliance, ICH-GCP standards, or clinical data management.
  • Experience across multiple therapeutic areas or global, multi-site trials.

Why this role stands out

  • Chance to work at the intersection of clinical research and advanced AI development.
  • Fully remote and flexible work arrangement.
  • Freelance-style autonomy with structured, task-based project work.
  • Exposure to advanced AI models trained on real clinical research data.
  • Opportunity to help improve how AI understands healthcare and clinical science.
  • Potential for continued assignments and contract extensions as new projects begin.

Additional information

This position is a paid hourly contract role. It is intended for independent, remote contributors who can handle flexible weekly availability within the stated commitment range.

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