Global Site Activation Lead

IQVIA

Doylestown (Bucks County)

On-site

USD 87,000 - 216,000

Full time

5 days ago
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Job summary

IQVIA, a global leader in clinical research services, seeks a Site Activation leader to drive strategic, operational, and financial delivery of Site Activation activities across multiple regions. You will oversee Site ID, site selection, ethics and regulatory processes, and contracting to enable rapid patient enrollment.

The role requires coordination with internal teams and sponsor requirements, ensuring compliance with ICH-GCP, timelines, and quality standards.

Qualifications

  • Bachelor's Degree in Life sciences or related field is required.
  • At least 5 years with 2 years of lead experience in a scientific or clinical environment.
  • Demonstrable experience in an international role or equivalent combination of education, training and experience.

Responsibilities

  • Provides strategic planning and project oversight to accelerate Site Activation for fast patient enrollment.
  • Oversee Start Up and Lifecycle Maintenance per approved strategy and timelines, compliant with ICH-GCP and protocols.
  • Collaborate with internal and external stakeholders across regions/countries to deliver project scope and maintain Site Activation Management Plan.
  • Manage regulatory strategy and submissions, including site approvals and essential document review/negotiation.
  • Provide updates to study teams and senior leadership while maintaining internal systems and project plans.

Skills

Project management
Leadership
Cross-functional collaboration

Education

Bachelor's Degree Life sciences or related field
5 years experience with 2 years lead experience
International role experience

Job description

IQVIA, a global leader in clinical research services, seeks a Site Activation leader to drive strategic, operational, and financial delivery of Site Activation activities across multiple regions. You will oversee Site ID, site selection, ethics and regulatory processes, and contracting to enable rapid patient enrollment.

The role requires coordination with internal teams and sponsor requirements, ensuring compliance with ICH-GCP, timelines, and quality standards.

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