Director, Clinical Operations

Disc Medicine

. Lead and direct execution of multiple global Phase 2/3 studies aligned with enrollment objectives and timelines .

Posted 9/24/2026full-timeWatertown • Massachusetts • United StatesLead💰 $207,000 - $253,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical trial management, with a strong focus on leading global Phase 2/3 studies, ensuring compliance with ICH-GCP standards, and managing cross-functional teams. Possesses advanced skills in data management and regulatory processes, complemented by exceptional leadership and communication abilities.

Highest-signal resume keywords

Clinical Trial ManagementICH-GCP ComplianceRegulatory Document AuthoringLeadership in Clinical OperationsBiotech Industry Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Development ProcessesElectronic Data SystemsKPI TrackingBudget ManagementStudy Plan Development

Soft Skills

Interpersonal SkillsOrganizational SkillsCommunication SkillsAdaptabilityBusiness Acumen

Tools & Technologies

Microsoft Office

Industry Keywords

BiotechPharmaceuticalCROOrphan IndicationsOncology

About the role

Key responsibilities & impact

Lead and direct execution of multiple global Phase 2/3 studies aligned with enrollment objectives and timelines
Manage trial managers and CTAs and provide expert counsel for issue resolution
Provide Clinical Operations leadership under the Executive Director of Clinical Development Operations
Contribute to Clinical Development Plans and associated operational strategy
Collaborate with Clinical Study Teams to develop and implement study plans
Oversee execution of assigned clinical programs, focusing on quality, budget, and timelines
Oversee Strategic Partners and other vendors to meet ICH-GCP obligations and business objectives
Track KPIs for study milestones and communicate program status, costs, and issues to senior management
Assist in authoring key regulatory documents and align clinical program deliverables with submission requirements and regulatory expectations
Collaborate with medical, regulatory affairs, data management, biostatistics, and medical affairs teams
Share learnings and best practices to enable process improvements
Monitor industry trends, emerging technologies, and innovative recruitment solutions
Perform other business needs identified by the direct line manager

Requirements

What you’ll need

BA/BS in relevant field required
Approximately 10 years of experience in trial management, preferably within the biotech, pharmaceutical, or CRO industry
Advanced skills in Microsoft Office programs
Good working knowledge of electronic data systems
Comprehensive understanding of clinical development processes, GCP, ICH, and global regulatory requirements
Must be willing to travel both domestic and international
Strong interpersonal skills to interact with investigators, vendors, and individuals at all levels of the organization
Exceptional leadership, communication, and organizational skills
Highly organized with a positive attitude; works well through change and shifting priorities
Strong business acumen, including in-depth knowledge of multidisciplinary drug development functions such as data management, biostatistics, regulatory, and pharmacovigilance
Experience in orphan indications or oncology will be favorably considered

Benefits

Comp & perks

Flexible work environment
Hybrid work arrangement with flexibility to work remotely or from headquarters
Comprehensive benefits
Competitive compensation packages
Equal-opportunity employment