Global Site Activation Lead: Fast Start-Up & Compliance

IQVIA Argentina

Wayne (NJ)

On-site

USD 60,000 - 157,000

Full time

12 days ago
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Job summary

IQVIA is seeking a Site Activation Lead to direct the execution of strategic, operational, and financial delivery of site activation activities across multiple countries within a region. You will ensure fast site activation for patient enrollment in alignment with the Site Activation Management Plan.

The role requires a Life Science degree, 3+ years in a clinical environment, and strong project management and regulatory knowledge.

Qualifications

  • Bachelor's Degree Life Science or related field.
  • 3+ years relevant experience in a scientific or clinical environment.
  • Demonstrable international/global role experience.
  • In-depth knowledge of clinical systems, procedures and regulatory standards.
  • Strong knowledge of medical terminology and regulations.
  • Proficient with Microsoft Office and email applications.

Responsibilities

  • Provide strategic planning and project oversight to accelerate site activation.
  • Oversee Start Up and lifecycle maintenance per strategy and timelines.
  • Collaborate with stakeholders across regions/countries to deliver project scope.
  • Develop, implement and maintain the Site Activation Management Plan.
  • Assess regulatory landscape and provide regulatory intelligence for studies.
  • Deliver presentations/trainings to clients and colleagues.
  • Maintain internal systems, databases, and project plans.

Skills

Strong communication
Organizational skills
Multi-project management

Education

Bachelor's Degree Life Science or related field

Tools

Microsoft Office

Job description

IQVIA is seeking a Site Activation Lead to direct the execution of strategic, operational, and financial delivery of site activation activities across multiple countries within a region. You will ensure fast site activation for patient enrollment in alignment with the Site Activation Management Plan.

The role requires a Life Science degree, 3+ years in a clinical environment, and strong project management and regulatory knowledge.

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