Senior Data Team Lead

IQVIA

Senior Data Team Lead overseeing end-to-end data management for global clinical trials at IQVIA. Leading cross-functional teams to ensure quality, accuracy, and compliance in clinical projects.

Posted 7/30/2026full-timeRemote • California, Florida, North Carolina, South Carolina, Virginia • 🇺🇸 United StatesSenior💰 $86,800 - $217,100 per yearWebsite

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 managing timelines, budgets, and resources effectively. Proven ability to mentor teams and drive process improvements in clinical data management.

Highest-signal resume keywords

Lead Clinical Data Management ExperienceExpertise With Medidata RaveExpertise With Oracle InFormUnderstanding Of GCPUnderstanding Of ICH

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ManagementData ReconciliationDatabase DeploymentProcess ImprovementRegulatory Compliance

Soft Skills

Excellent CommunicationLeadership SkillsMentoring

Tools & Technologies

Medidata RaveOracle InForm

Industry Keywords

Clinical TrialsGlobal StudiesSAEPKSOP Compliance

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 7 years of direct clinical data management experience
5+ years in a Lead Clinical Data Management role REQUIRED
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
An equivalent combination of education, training, and experience may be considered

Benefits

Comp & perks

Fully remote role – company equipment provided
Competitive salary and performance-based incentives
Medical, dental, and vision coverage beginning your first day of employment
401(k) with company match, life insurance, and discretionary PTO
Career growth and learning opportunities through mentoring and internal mobility
Inclusive, global culture focused on innovation and collaboration