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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading global cardiovascular clinical trials, managing study budgets, timelines, and vendor relationships while ensuring compliance with ICH-GCP and clinical trial regulations. Proven ability to drive study quality, risk management, and operational reporting in a cross-functional team environment.
Highest-signal resume keywords
Global Clinical Study LeadershipICH-GCP KnowledgeStudy Budget ManagementVendor ManagementCardiovascular Clinical Trials Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ManagementRisk ManagementOperational ReportingStudy PlanningIssue Resolution
Soft Skills
LeadershipStakeholder ManagementCommunicationOrganisational Skills
Certifications & Qualifications
Project Management Certification
Industry Keywords
Life SciencesClinical ResearchPharmaceutical DevelopmentBiotechnologyCardiometabolic Trials
About the role
Key responsibilities & impact- Lead global study teams to deliver cardiovascular clinical trials across the study lifecycle
- Drive study timelines, budgets, quality objectives, and key milestones
- Serve as the primary operational contact for study teams, CROs, and external partners
- Oversee outsourced activities, ensuring effective vendor management and study oversight
- Lead study planning, risk management, issue resolution, and escalation activities
- Ensure TMF quality and inspection readiness
- Manage study budgets, forecasting, and operational reporting
- Support audits, regulatory inspections, and process improvement initiatives
- Lead delivery of global cardiovascular and cardiometabolic clinical trials
Requirements
What you’ll need- Degree in Life Sciences, Clinical Research, or a related field
- Significant global experience within pharmaceutical or biotechnology clinical development
- Proven experience leading global clinical studies and cross-functional teams
- Strong knowledge of ICH-GCP, clinical trial regulations, and study management principles
- Experience managing study budgets, vendors, timelines, and operational risks
- Excellent leadership, stakeholder management, communication, and organisational skills
- Experience supporting cardiovascular or cardiometabolic clinical trials is highly desirable
- Advanced degree (Master's, PhD, or equivalent) preferred
- Project Management certification preferred
- Experience delivering large-scale global studies across multiple phases of development preferred
- Previous involvement in cardiovascular outcomes studies or late-phase cardiovascular trials advantageous
- Legal right to work in France
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways