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BeOne Medicines

Director, GCO Program Lead

BeOne Medicines

Director, GCO Program Lead responsible for strategic operational planning and clinical operational performance at BeOne. Managing global teams and ensuring project success in clinical trials.

Posted 7/29/2026full-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 expertise in managing global clinical trial programs, including strategic planning, budget management, and compliance with ICH/GCP Guidelines. Proven ability to lead and develop teams while ensuring project delivery and goal achievement across multiple regions.

Highest-signal resume keywords
Clinical Trial ManagementProject ManagementPeople ManagementICH/GCP Guidelines ExpertiseBudget Management

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ExecutionStrategic PlanningBudget ForecastingRegulatory ComplianceProgram Management
Soft Skills
Team LeadershipCollaborationCommunication
Industry Keywords
Clinical Trial IndustryHealthcare DisciplineMulti-Region TrialsEarly PlanningRegulatory Requirements

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Accountable and responsible for building, developing and retaining the global team of gCSM
  • Oversee the delivery and goal achievement of projects within the designated program(s)
  • Collaborate with other GCPLs to define and implement strategies and key priorities across-programs
  • Evaluate and develop strategic feasibility and budget estimates during Early Planning for new CDPs
  • Create and be accountable for the annual program budget and resource forecasts

Requirements

What you’ll need
  • Bachelor or higher degree in a scientific or healthcare discipline
  • 10+ years’ experience in clinical trial industry
  • Project management exposure/experience across the entire lifecycle of multi-region/country clinical trials
  • Experience in both people management and program management preferred
  • Expert knowledge on the execution of clinical trials through a deep understanding of ICH/GCP Guidelines and other applicable regulatory requirements

Benefits

Comp & perks
  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness