Global Site Activation & Start-Up Manager

IQVIA Inc; Bogotá; On-site; COP 180,000,000 - 250,000,000; Full time

Job summary

IQVIA is seeking a hands-on professional in Bogotá to lead site activation and maintenance for multi-protocol clinical studies. You will coordinate regulatory submissions, ensure timelines, and manage cross-regional collaboration to support study initiation and ongoing maintenance.

Responsibilities include directing regulatory strategy, overseeing documentation, and mentoring junior staff within a global study-management framework.

Qualifications

• Regulatory and clinical trial start-up experience preferred.
• Ability to manage multi-regional programs and budgets.

Responsibilities

• Oversee site activation and maintenance activities per plan and timelines.
• Develop and maintain project plans and documentation; ensure regulatory compliance.

Skills

Regulatory affairs

Project management

Tools

CTMS

Job description

IQVIA is seeking a hands-on professional in Bogotá to lead site activation and maintenance for multi-protocol clinical studies. You will coordinate regulatory submissions, ensure timelines, and manage cross-regional collaboration to support study initiation and ongoing maintenance.

Responsibilities include directing regulatory strategy, overseeing documentation, and mentoring junior staff within a global study-management framework.