Global Site Activation Lead

IQVIA; Durham (NC); On-site; USD 60,000 - 157,000; Full time

Job summary

IQVIA is seeking a Site Activation Director to lead strategic and operational delivery for assigned studies, overseeing Site ID, site selection, and regulatory contracting. You will ensure timelines and quality while coordinating across regional teams to enable patient enrollment.

The role requires a life sciences degree and 3+ years in a clinical setting, with strong knowledge of ICH-GCP and regulatory standards, and excellent cross-functional communication.

Qualifications

• Bachelor's degree in Life Science or related field.
• At least 3 years in a scientific or clinical environment.
• Experience in an international role or cross-border projects.
• Knowledge of clinical systems, procedures and standards.
• Strong understanding of medical terminology and regulations.
• Broad knowledge of clinical research.

Responsibilities

• Direct and manage Site Activation activities (Site ID, selection, ethics/regulatory processes).
• Oversee Start Up and Lifecycle Maintenance per plan and timelines.
• Collaborate with internal/external stakeholders across regions to deliver scope.
• Prepare and maintain Site Activation Management Plan.
• Provide updates and reporting to study teams and senior colleagues.
• Ensure regulatory intelligence and contract documents are accurate.

Skills

Strategic planning

Project oversight

Communication

Independence

Education

Bachelor's degree Life Science

Tools

Microsoft Office

Job description

IQVIA is seeking a Site Activation Director to lead strategic and operational delivery for assigned studies, overseeing Site ID, site selection, and regulatory contracting. You will ensure timelines and quality while coordinating across regional teams to enable patient enrollment.

The role requires a life sciences degree and 3+ years in a clinical setting, with strong knowledge of ICH-GCP and regulatory standards, and excellent cross-functional communication.