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IQVIA

Clinical Lead – Global Study Leadership

IQVIA

. Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectives .

Posted 10/14/2026full-timeBuenos Aires • ArgentinaSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in leading clinical study delivery, ensuring adherence to quality standards, regulatory requirements, and operational excellence. Proficient in stakeholder management, financial oversight, and driving patient recruitment strategies to achieve study objectives.

Highest-signal resume keywords
Clinical Research ExperienceICH-GCP GuidelinesPatient Recruitment StrategiesCross-Functional CollaborationFinancial Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial ConductClinical OperationsSite ManagementQuality OversightResource PlanningProject DeliveryRisk ManagementBudget ManagementOperational PlanningProposal Development
Soft Skills
Strong CommunicationProblem-SolvingOrganizational SkillsDecision-MakingLeadership
Industry Keywords
Life SciencesHealthcareCROPharmaceuticalBiotechnologyClinical DeliveryStakeholder EngagementContinuous ImprovementKnowledge SharingGlobal Environment

About the role

Key responsibilities & impact
  • Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectives
  • Drive patient recruitment and site engagement strategies, ensuring enrolment targets are achieved and studies remain on track
  • Partner with Project Leaders and cross-functional teams to drive study milestones, resolve issues and maintain operational excellence
  • Provide leadership and guidance to clinical teams, supporting resource planning, training and project delivery
  • Manage clinical risks, oversee quality standards and drive proactive mitigation strategies throughout the study lifecycle
  • Build strong relationships with internal and external stakeholders, ensuring effective communication and alignment across study teams
  • Support financial oversight of clinical delivery, including forecasting, budget management and identification of scope changes where applicable
  • Contribute to continuous improvement initiatives, knowledge sharing and the development of less experienced team members
  • Support proposal development, bid defence activities and clinical delivery planning for new opportunities where appropriate

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline
  • 5+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment
  • Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
  • Experience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversight
  • Proven ability to collaborate across cross-functional teams and manage internal and external stakeholders in a global environment
  • Strong communication, problem-solving, organizational and decision-making skills
  • Experience supporting project financial management and operational planning is desirable
  • Passion for advancing clinical research and improving outcomes for patients worldwide