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IQVIA

Senior Data Management Lead

IQVIA

Data Management Lead overseeing data management delivery for global clinical trials at IQVIA. Ensuring quality, accuracy, and compliance while leading cross-functional teams for new therapies.

Posted 7/13/2026full-timeRemote • 🇿🇦 South AfricaSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates extensive expertise in leading data management for global clinical trials, ensuring compliance with GCP and ICH standards while effectively managing timelines, budgets, and resources. Proven ability to mentor teams and drive process improvements in clinical data management.

Highest-signal resume keywords
Lead Clinical Data ManagementClinical Data Management ExperienceMedidata RaveOracle InFormGCP Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Data ManagementDatabase LockSAE ReconciliationPK ReconciliationDatabase DeploymentProcess ImprovementsResource AllocationTimelines ManagementBudget ManagementClinical Research Processes
Soft Skills
Excellent CommunicationLeadership SkillsMentoring
Tools & Technologies
EDC Systems
Industry Keywords
Clinical TrialsLife SciencesHealthBiological FieldMathematical FieldICH Standards

Tech Stack

Tools & technologies
Google Cloud PlatformOracle

About the role

Key responsibilities & impact
  • Lead data management for complex, global clinical trials from study setup to database lock
  • Serve as the main client contact for all data management deliverables
  • Oversee SAE, PK, and external data reconciliation and database deployment
  • Manage timelines, budgets, and resource allocation to meet customer expectations
  • Mentor junior data management staff and promote best practices
  • Drive process improvements and ensure regulatory and SOP compliance

Requirements

What you’ll need
  • Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field
  • No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role
  • Proven success managing large global studies (1000+ patients)
  • Expertise with Medidata Rave, Oracle InForm, or similar EDC systems
  • Strong understanding of GCP, ICH, and clinical research processes
  • Excellent communication and leadership skills.

Benefits

Comp & perks
  • Fully remote role – company equipment provided
  • Competitive salary and performance-based incentives
  • Career growth and learning opportunities through mentoring and internal mobility
  • Inclusive, global culture focused on innovation and collaboration