Director, Clinical Operations – Home-Based
Location: Durham, North Carolina (Additional locations available)
Job Type: Full-Time | Remote
Requisition ID: R1492826
Company: IQVIA
Salary:
$119,400 – $332,500 annually
(Compensation will vary based on experience, education, location, and additional role-specific factors. May include incentive plans and benefits.)
Position Overview:
IQVIA is hiring a Director of Clinical Operations to lead, develop, and oversee clinical monitoring functions across a designated region or group. This strategic role ensures high-quality clinical delivery, team performance, training, resource planning, and client engagement. The position reports to senior regional leadership and supports initiatives aligning clinical operational execution with company-wide objectives.
Key Responsibilities:
Team Management: Lead a team of Clinical Research Specialists (CRSs), Associate Directors, and Managers
Hiring & Onboarding: Direct hiring, interviewing, and onboarding processes for clinical staff
Training Oversight: Implement training plans, SOP reviews, and mentoring programs
Resource Planning: Forecast and manage regional clinical resourcing needs in collaboration with study leads
Quality & Metrics Review: Evaluate workload, performance metrics, and implement quality improvements
Budget Oversight: Review and analyze clinical study budgets and ensure fiscal discipline
Client Engagement: Serve as client liaison and interface with key stakeholders on clinical deliverables
Cross-Functional Collaboration: Partner with project managers, business development, and operational leads
Leadership Development: Mentor junior leaders and guide professional growth initiatives
Strategic Participation: Lead or participate in global process improvement and quality initiatives
Travel Requirement: ~30–40% travel for project oversight and leadership engagements
Required Qualifications:
Bachelor's degree in a healthcare or scientific discipline (or equivalent education/experience)
12+ years of experience in clinical trials, including 7+ years in leadership roles
Deep understanding of ICH-GCP, regulatory requirements, and clinical project execution
Strong financial and operational acumen in clinical research management
Proficiency in MS Word, Excel, PowerPoint, and clinical systems
Outstanding communication, presentation, problem-solving, and time-management skills
Preferred Attributes:
Advanced degree (MS, MPH, MBA)
Experience in managing multinational trials or cross-regional clinical teams
Proven success in client-facing roles and team leadership in a matrixed environment
Physical Requirements:
Extensive use of phone and computer
Sitting for extended periods
Repetitive keyboard usage
Willingness to travel as required
Gujarat :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
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Queensland |Melbourne :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Canada |Quebec :
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Koropi | Athens |Greece :
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Auckland |New Zealand :
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Manila |Croatia :
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