Hybrid Director, Clinical Operations – Global Trials

Disc Medicine; Massachusetts; Hybrid; USD 207,000 - 253,000; Full time

Benefits offered by this job

Health insurance

Job summary

Disc Medicine is seeking a Director of Clinical Operations in a dynamic hybrid role with the flexibility to work remotely or from our Watertown, MA headquarters. You will report to the Executive Director, Clinical Development Operations and lead multiple Phase 2/3 trials, managing trial managers and vendors to ensure timely, on-budget execution.

The position requires a strong track record in clinical development, excellent communication, and the ability to collaborate with regulatory, data

Qualifications

• BA/BS in a relevant field is required.
• Minimum of about 10 years in trial management within biotech/pharma/CRO.
• Strong leadership, communication, and organizational skills are essential.

Responsibilities

• Lead the execution of multiple global Phase 2/3 studies aligned with timelines.
• Manage trial managers and CTAs and provide expert issue resolution.
• Provide Clinical Operations leadership under the Executive Director.
• Develop and implement study plans with Clinical Study Teams.
• Ensure quality, budget and timelines for assigned programs.
• Oversee vendors and strategic partners to meet ICH-GCP objectives.
• Monitor KPIs and communicate status to senior management.
• Contribute to regulatory deliverables and submission readiness.
• Collaborate with regulatory, data mgmt, biostats and medical affairs teams.
• Share learnings to drive process improvements.

Skills

Leadership

Trial management

Regulatory knowledge

Communication

Project management

Education

BA/BS in relevant field

Tools

Microsoft Office

EDC systems

Job description

Disc Medicine is seeking a Director of Clinical Operations in a dynamic hybrid role with the flexibility to work remotely or from our Watertown, MA headquarters. You will report to the Executive Director, Clinical Development Operations and lead multiple Phase 2/3 trials, managing trial managers and vendors to ensure timely, on-budget execution.

The position requires a strong track record in clinical development, excellent communication, and the ability to collaborate with regulatory, data