Global Clinical Program Lead - MedTech Studies

IQVIA Argentina; Washington (District of Columbia); On-site; USD 140,000 - 233,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Project Manager to lead global MedTech clinical studies, coordinating sponsors and cross-functional teams to deliver on time, within budget, and in compliance with regulatory and quality standards. The role provides strategic leadership across multi-country programs to drive operational excellence and successful outcomes.

You will mentor staff, manage timelines and budgets, support regulatory submissions, and deliver regular updates to sponsors and internal

Qualifications

• Minimum 7 years in clinical research, including at least 4 years in clinical project management.
• Experience managing global multi-country clinical studies.
• Experience supporting regulatory submissions and cross-functional collaboration.

Responsibilities

• Lead planning, execution, and delivery of global MedTech clinical studies.
• Serve as primary sponsor contact and maintain client relationships.
• Develop and manage study timelines, budgets, forecasts, and risk plans.
• Lead cross-functional teams to meet milestones and study objectives.
• Monitor progress, escalate risks, and resolve issues.
• Ensure ICH-GCP, ISO 14155, regulatory and quality compliance.
• Collaborate with operations, data management, biostatistics, regulatory, safety, and others.
• Manage study finances, including forecasting, scope, and profitability.
• Support bid defenses and new business opportunities.
• Drive process improvement and share lessons learned.

Skills

Clinical trial mgmt

Global teams leadership

Client relationships

Budget & forecasting

Regulatory knowledge

Project planning

Quality assurance

Stakeholder management

Education

Bachelor's in Life Sciences/Healthcare

Tools

CTMS

MS Office

Job description

IQVIA is seeking a Senior Clinical Project Manager to lead global MedTech clinical studies, coordinating sponsors and cross-functional teams to deliver on time, within budget, and in compliance with regulatory and quality standards. The role provides strategic leadership across multi-country programs to drive operational excellence and successful outcomes.

You will mentor staff, manage timelines and budgets, support regulatory submissions, and deliver regular updates to sponsors and internal