Senior Global Clinical Trial Delivery Lead

IQVIA; Warszawa; On-site; PLN 218,000 - 405,000; Full time

Job summary

IQVIA in Warszawa is seeking a Senior Global Trial Manager to lead the clinical delivery of large, multi-regional studies in line with GCP and SOPs. You will collaborate with clinical teams to ensure on-time and compliant trial execution and report to stakeholders as required.

The role requires strong project-management skills, solid clinical research background, and ability to manage budgets and risks. You may mentor peers and contribute to business development activities as needed.

Qualifications

• 3–5 years of prior relevant experience.
• Bachelor's degree in health care or other scientific discipline is required.
• Requires 7 years clinical research/monitoring experience or equivalent combination of education, training and experience.
• Requires knowledge of project management practices and terminology.

Responsibilities

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH GCP, protocol), contract, and SOPs.
• Accountable for meeting projects' clinical targets.
• Contribute to the development of the project risk mitigation plan and manage clinical risks through the lifecycle.
• Ensure clinical quality by identifying standards and monitoring compliance and issues.
• Lead the client relationship as primary point of contact and manage stakeholder communications.
• Oversee resourcing and talent planning of the clinical team for on-time delivery.
• Mentor and coach new peers and participate in bid defense preparations as needed.

Skills

GCP/ICH knowledge

Project management

Stakeholder management

Clinical research experience

Education

Bachelor's degree in healthcare or scientific discipline

Job description

IQVIA in Warszawa is seeking a Senior Global Trial Manager to lead the clinical delivery of large, multi-regional studies in line with GCP and SOPs. You will collaborate with clinical teams to ensure on-time and compliant trial execution and report to stakeholders as required.

The role requires strong project-management skills, solid clinical research background, and ability to manage budgets and risks. You may mentor peers and contribute to business development activities as needed.