Director, GCO Program Lead

BeOne Medicines

. Lead strategic operational planning and clinical operational performance for designated programs .

Posted 11/5/2026full-timeRemote • United StatesSenior💰 $171,900 - $231,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in clinical operations management, project management, and resource allocation within the clinical trial industry, particularly in lung cancer. Proven ability to lead teams, mentor talent, and drive strategic operational planning and performance.

Highest-signal resume keywords

Clinical Operations ManagementProject ManagementPeople ManagementICH/GCP GuidelinesLung Cancer Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical DocumentationData ManagementRisk ManagementResource ManagementContract ManagementFeasibility StudiesTechnical ReportingProject/Program DesignBudget CreationOperational KPI Tracking

Soft Skills

MentorshipCollaborationLeadership

Tools & Technologies

Microsoft Office

Industry Keywords

Clinical Trial IndustryGlobal EnvironmentStudy PlanningProgram Review MeetingsVendor Governance

About the role

Key responsibilities & impact

Lead strategic operational planning and clinical operational performance for designated programs
Act as escalation point for study and compound-related issues
Lead gCSMs and provide mentorship, talent development, performance management, and resource management
Partner with program leads and functional representatives to drive disease and asset strategy
Provide clinical operational insight to governance teams and support program strategy
Lead or participate in KOL engagement activities
Evaluate strategic feasibility and budget estimates for new clinical development plans and strategy changes
Allocate resources and initiate CST formation
Create annual program budgets and resource forecasts
Create, review, maintain, and provide input on compound-level documents including IB, DSUR, and protocols
Oversee study planning and execution within the designated program
Conduct program review meetings and track studies against approved budgets and timelines
Report study status, goals, operational KPIs, and quality KPIs
Evaluate preferred global vendors and participate in vendor governance meetings
Provide line management and mentorship to gCSMs
Drive scientific knowledge development and process improvement within Clinical Operations
Collaborate with cross-functional leaders to support clinical development goals

Requirements

What you’ll need

Bachelor or higher degree in a scientific or healthcare discipline
10+ years’ experience in the clinical trial industry
Lung cancer experience
Project management exposure/experience across the entire lifecycle of multi-region/country clinical trials in a fast-paced global environment
Experience in people management and program management preferred
Microsoft Office skills
Deep understanding of ICH/GCP Guidelines and other applicable regulatory requirements
Clinical documentation and records management
Clinical operations management
Contract management
Data management
Feasibility studies
Project/program design
Project/program management
Risk management
Technical reporting
Resource management
Travel may be required as per business need

Benefits

Comp & perks

Annual bonus plan eligibility for non-commercial roles
Incentive compensation plan eligibility for commercial roles
Discretionary equity awards
Employee Stock Purchase Plan
Medical insurance
Dental insurance
Vision insurance
401(k)
FSA/HSA
Life insurance
Paid Time Off
Wellness benefits