Global Clinical Operations Director - Hybrid/Remote

Disc Medicine

United States

Hybrid

USD 207,000 - 253,000

Full time

3 days ago
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Benefits offered by this job

Flexible hybrid work
HQ in Watertown, MA

Job summary

Disc Medicine is hiring a Director, Clinical Operations in a dynamic hybrid role that offers flexibility to work remotely or from our Watertown, MA headquarters. This position leads global Phase 2/3 trials, manages trial managers, and partners with stakeholders to ensure strategic execution in a fast-paced biotech environment.

The role requires ~10 years in trial management, strong leadership, and regulatory know-how.

Qualifications

  • Extensive trial management experience in biotech/pharma or CRO environments.
  • Strong leadership, communication, and organizational skills.
  • Proficient with Microsoft Office and electronic data systems.
  • Willingness to travel domestically and internationally.

Responsibilities

  • Lead and direct the execution of multiple global Phase 2/3 studies aligned with enrollment objectives and timelines.
  • Line management of trial managers and CTAs; provide expert counsel for issue resolution.
  • Provide Clinical Operations leadership to support development plans and operational strategy.
  • Collaborate with cross-functional teams to ensure cohesive and compliant trial delivery.
  • Oversee budgets, timelines, and vendor relationships to meet ICH-GCP and business objectives.
  • Track KPIs and report program status, costs, and risks to senior leadership.
  • Assist in authoring regulatory documents and ensure alignment with submissions.

Education

BA/BS in relevant field

Tools

Electronic data capture systems

Job description

Disc Medicine is hiring a Director, Clinical Operations in a dynamic hybrid role that offers flexibility to work remotely or from our Watertown, MA headquarters. This position leads global Phase 2/3 trials, manages trial managers, and partners with stakeholders to ensure strategic execution in a fast-paced biotech environment.

The role requires ~10 years in trial management, strong leadership, and regulatory know-how.

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