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IQVIA

Clinical Project Manager – Global Study Leadership

IQVIA

. Lead the delivery of regional and global clinical studies or assigned study workstreams from start-up through close-out .

Posted 11/9/2026full-timeMadrid • SpainSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in leading clinical studies and managing project timelines, budgets, and quality within compliance frameworks. Proven ability to build strong relationships with sponsors and stakeholders while driving successful study outcomes.

Highest-signal resume keywords
Clinical Research ExperienceProject ManagementICH-GCP GuidelinesStakeholder Relationship ManagementRisk Mitigation

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
Study Management PlansClinical Trial ConductBudget ManagementOperational Performance ManagementIssue Resolution
Soft Skills
Strong CommunicationCollaborationProblem-SolvingDecision-Making
Industry Keywords
Life SciencesHealthcareCROPharmaceuticalBiotechnologyRegulatory RequirementsSOPsContinuous Improvement

About the role

Key responsibilities & impact
  • Lead the delivery of regional and global clinical studies or assigned study workstreams from start-up through close-out
  • Build strong relationships with sponsors, serving as a primary or key project contact and ensuring an exceptional customer experience
  • Lead and coordinate cross-functional teams to achieve project milestones and study objectives
  • Develop and execute study management plans to support successful study delivery
  • Manage study timelines, budgets, quality, risks and operational performance throughout the project lifecycle
  • Drive proactive issue resolution, risk mitigation and stakeholder alignment to ensure successful study outcomes
  • Support financial oversight, forecasting, change control and vendor management activities where applicable
  • Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements, SOPs and contractual commitments
  • Contribute to continuous improvement through lessons learned, best-practice sharing and support of developing team members

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline
  • 5+ years of clinical research experience, including project management experience within a CRO, pharmaceutical, or biotechnology environment
  • Experience leading clinical studies, study workstreams, or cross-functional project teams
  • Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
  • Proven ability to manage study timelines, risks, quality, budgets and operational performance
  • Experience building effective sponsor and stakeholder relationships within a global environment
  • Strong communication, collaboration, problem-solving and decision-making skills
  • Ability to thrive in a fast-paced, matrixed environment while balancing multiple priorities
  • Passion for advancing clinical research and improving patient outcomes

Benefits

Comp & perks
  • Flexible ways of working
  • Mentorship
  • Opportunities for professional development and career growth
  • Exposure to diverse clinical studies and therapeutic areas
  • Collaboration with experienced project leaders and cross-functional experts
  • AI-enabled technology and data-driven insights
  • Supportive collaborative global network