Senior Clinical Program Lead – Early Development

IQVIA; Oeiras; On-site; EUR 60,000 - 90,000; Full time

Job summary

IQVIA is seeking a Senior CPM to lead clinical study delivery within a global CRO framework. You will manage cross-functional teams, supervise project execution, and ensure timely, high-quality outcomes aligned with contracts and SOPs.

Key focus areas include risk management, bid defense participation, strategic planning, and maintaining strong customer relationships while driving efficiency and cost controls across multi-regional studies.

Qualifications

• Bachelor's degree in life sciences required.
• 5+ years in clinical research with 4+ years in PM.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Excellent written and verbal English.

Responsibilities

• Lead bid defense preparations and presentations.
• Develop integrated study management plans.
• Oversee contract-driven study delivery and quality.
• Manage cross-functional teams to meet milestones.
• Monitor progress and communicate with stakeholders.

Skills

Project leadership

Clinical project management

Bid defense

Cross-functional collaboration

English communication

Education

Bachelor's Degree Life sciences

Tools

MS Office

Clinical trial software

Job description

IQVIA is seeking a Senior CPM to lead clinical study delivery within a global CRO framework. You will manage cross-functional teams, supervise project execution, and ensure timely, high-quality outcomes aligned with contracts and SOPs.

Key focus areas include risk management, bid defense participation, strategic planning, and maintaining strong customer relationships while driving efficiency and cost controls across multi-regional studies.