Clinical Trial Program Lead

Eli Lilly and Company

Clinical Trial Program Lead guiding Lilly’s exploratory and biopharmaceutics clinical development programs. Overseeing Phase 1 trials, vendors, timelines, budgets, and regulatory milestones.

Posted 8/12/2026full-timeBracknell • 🇬🇧 United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading clinical development plans and managing Phase 1 clinical studies, with a strong focus on project management, vendor relationships, and regulatory compliance. Proven ability to mentor teams and communicate effectively across diverse stakeholders.

Highest-signal resume keywords

Clinical Development LeadershipPhase 1 Study ManagementVendor ManagementProject Management ToolsClinical Trial Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementBiopharmaceutics DevelopmentRegulatory Document PreparationBudget ManagementPatient Recruitment StrategiesTimeline CreationRisk Mitigation PlanningRoot Cause AnalysisMicrosoft Office SuiteProject Management Methodologies

Soft Skills

LeadershipMentoringEffective CommunicationProblem-SolvingAdaptability

Tools & Technologies

Project Management ToolsEnd-User Computing

Industry Keywords

Pharmaceutical IndustryClinical Research TrialsExploratory StudiesCross-Cultural TeamworkClinical Governance

About the role

Key responsibilities & impact

Lead the creation and execution of exploratory and biopharmaceutics clinical development plans at the molecule level
Provide technical leadership and operational oversight for clinical research trials
Plan and deliver clinical molecules and submission milestones on time and on budget throughout the molecule lifecycle
Manage global clinical trial operations from trial design through execution and closeout
Create and manage timelines, outsourcing plans, vendor relationships, patient recruitment and retention, and budgets
Lead Phase 1 clinical asset strategy and advise on clinical and regulatory documents
Stay current on disease knowledge, competitors, and industry trends
Lead clinical project management processes and tools
Collaborate with TPOs to execute clinical strategy and oversee trial outcomes
Identify and communicate clinical risks and mitigation plans
Oversee clinical trial planning and execution to meet timelines and budgets
Select and manage vendors and resolve operational issues
Partner with regulatory and medical teams on safety processes
Lead clinical team interactions and governance participation
Communicate across levels and functions to support decision-making
Mentor colleagues and provide constructive feedback

Requirements

What you’ll need

Bachelor’s degree in a science related field
Few years of experience in the pharmaceutical industry managing clinical studies
Few years of experience managing Phase 1 studies, including exploratory and biopharmaceutics clinical development
Experience with vendor and contract management
Proficiency in end-user computing and Microsoft Office (Word, Excel, PowerPoint, Project)
Strong knowledge of clinical trial regulations and guidelines
Experience managing TPOs to ensure trial deliverables
Experience with project management tools and methodologies
Willingness to travel up to 10%
Ability to mentor and develop others
Ability to work effectively in cross-cultural and virtual team environments
Strong leadership and networking capabilities
Root cause analysis and problem-solving skills
Effective time management and adaptability to diverse stakeholders
Clear written and verbal communication skills
Ability to influence and build strong internal and external relationships

Benefits

Comp & perks

Travel opportunities up to 10%
Mentoring and development opportunities
Accommodation support for applicants with disabilities
Inclusive culture supporting diversity, integrity, excellence, and respect for people