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Job description
Key Responsibilities
Lead and develop trial management leaders, setting clear expectations for performance, collaboration, and execution
Standardize and continuously improve trial management best practices, tools, and operating rhythms across programs
Drive harmonization of trial management processes across Verve and Lilly to support a consistent and scalable operating model
Serve as an active member of the Clinical Development Operations leadership team, contributing to strategic planning, organizational effectiveness, and functional direction
Provide oversight across clinical programs to ensure delivery against timelines, quality expectations, budgets, and study goals
Partner closely with cross-functional teams (Clinical Development, Regulatory, Data Management, Patient recruitment/retention, Study start up, Medical Writing, Supply Chain, Quality, Clinical Compliance, etc.) to support aligned study execution
Strengthen governance, escalation, and decision-making with Compliance and Oversight to identify and address operational risks early
Ensure teams apply a risk-based approach to planning, study oversight, and issue resolution
Oversee CRO and vendor strategy, including performance, partnership, and accountability
Support development/refinement of SOPs, workflows, and business processes promoting quality, compliance, and consistency
Champion compliance with GCP, ICH, and applicable global regulatory requirements; support inspection readiness
Monitor operational metrics and use data-driven insights to improve execution and resource planning
Foster a culture of collaboration, accountability, inclusion, and continuous improvement
Coach, mentor, and develop trial management talent
Represent the trial management function in cross-functional and leadership forums
Basic Qualifications
Bachelor’s degree in a scientific, healthcare, or related discipline required; advanced degree preferred
Significant clinical operations or trial management experience within a sponsor organization
Additional Skills/Preferences
Proven success leading leaders and building high-performing teams in a matrixed clinical development environment
Strong experience overseeing global clinical trials across multiple phases
Deep understanding of GCP, ICH, and applicable regulatory requirements
Ability to standardize processes, implement operational improvements, and lead through changeStrong critical thinking, judgment, and problem-solving
Ability to balance strategic leadership with operational execution
Experience supporting organizational integration, process harmonization, or operating model evolution preferred
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.