Global MedTech Clinical Program Lead

IQVIA; Washington (District of Columbia); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Project Manager to lead global MedTech clinical studies, coordinating cross‑functional teams across regions to ensure on‑time, on‑budget delivery with regulatory compliance. You will serve as the primary sponsor contact and drive continuous improvement across study programs.

The role requires 7+ years in clinical research, including 4+ years in project management, and a strong track record in multi-country studies and stakeholder management.

Qualifications

• Bachelor’s degree in life sciences or related field required.
• Minimum 7 years in clinical research with 4+ years in project management.
• Experience leading global, multi-country clinical studies across regions.
• Strong knowledge of ICH-GCP, ISO 14155 and regulatory requirements.
• Proven ability to manage budgets, forecasting, and contracts.

Responsibilities

• Lead planning, execution, and delivery of global MedTech clinical studies.
• Serve as primary contact for sponsors and maintain client relationships.
• Develop study timelines, budgets, forecasts, and risk plans.
• Lead cross-functional teams to meet milestones and objectives.
• Monitor progress, escalate risks, and ensure quality standards.
• Ensure compliance with ICH-GCP, ISO 14155, and regulatory requirements.
• Collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Safety, and others.
• Manage study finances, including forecasting and change orders.
• Support bid defenses and business development activities.

Skills

Clinical trial management

Cross-functional leadership

Client relationship management

Regulatory compliance

Strategic project leadership

Education

Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, Healthcare, or related discipline

Tools

Clinical trial management systems

Microsoft Office

Job description

IQVIA is seeking a Senior Clinical Project Manager to lead global MedTech clinical studies, coordinating cross‑functional teams across regions to ensure on‑time, on‑budget delivery with regulatory compliance. You will serve as the primary sponsor contact and drive continuous improvement across study programs.

The role requires 7+ years in clinical research, including 4+ years in project management, and a strong track record in multi-country studies and stakeholder management.