Associate Clinical Lead Director, Project Oversight
Durham, North Carolina (Home-based)
Job ID: R1494446
Job Type: Full-Time
Work Arrangement: Remote (with up to 25% travel)
Available In: Additional locations
As an Associate Clinical Lead Director, you’ll play a key leadership role in clinical trial delivery. You will guide clinical teams, ensuring regulatory compliance, client satisfaction, and successful trial execution. This role supports large, multi-regional studies or a program of studies and works closely with Project Leaders and cross-functional teams.
Ensure delivery of assigned projects in compliance with:
ICH-GCP, protocols, contracts, SOPs, and policies
Accountable for meeting recruitment targets and implementing effective recruitment strategies
Manage clinical risks and contribute to risk mitigation planning
Define and execute clinical strategies aligned with project goals
Oversee and ensure clinical quality delivery, identifying standards and compliance measures
Manage clinical project finances including:
Estimate at Completion (EAC) planning and tracking
Monitoring scope changes and identifying out-of-scope work
Serve as primary Clinical Lead or as part of a broader clinical lead team for large, global trials
Identify and manage internal and external stakeholders
Coordinate project milestones and provide updates to stakeholders
Lead resourcing and talent planning for the clinical team
Provide guidance through operational plans and project-specific training
Conduct team meetings, support communication, and foster alignment with goals
Offer performance feedback to line managers regarding clinical team members
Support and mentor new clinical leads during onboarding
May serve as liaison for cross-functional departments or act as a change agent
Participate in and champion corporate initiatives or special projects
Contribute to proposal development and attend bid defense meetings
Present Clinical Operations Plans in collaboration with BD and project leadership
Up to 25% (domestic or international)
Bachelor’s Degree in health care, life sciences, or related field (required)
10+ years of clinical research or monitoring experience
In-depth knowledge of GCP, ICH guidelines, and clinical trial conduct
Familiarity with project management practices and terminology
Solid understanding of project financials
Experience working in global/multi-regional clinical trials
Proficient in Microsoft Office (Word, Excel, PowerPoint)
Strong IT literacy and ability to work with clinical trial systems
Excellent written and verbal communication skills
Comfortable presenting strategies and plans to internal and external audiences
Strong influencing, decision-making, and mentoring abilities
Experience leading diverse teams across multiple geographies
Skilled in building effective working relationships and managing cross-functional dynamics
High attention to detail and accuracy
Excellent time management and ability to prioritize conflicting demands
Client Focus
Communication
Innovation
Ownership
Collaboration
Base Salary Range (Annualized):
$102,500 – $285,500 (dependent on location, experience, and qualifications)
May include:
Incentive plans
Bonuses
Comprehensive health and welfare benefits
IQVIA is a global leader in clinical research, analytics, and healthcare data solutions. We accelerate innovation and help bring life-changing treatments to patients faster by connecting advanced analytics, technology, and expertise.
🔗 Learn more about IQVIA Careers
IQVIA is an Equal Opportunity Employer. All applicants will receive equal consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other protected status under applicable law.
🔗 Equal Employment Opportunity Policy
Apply online using Job ID: R1494446
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