Senior Site Activation Lead (Clinical Trials)

IQVIA Inc; Durham (NC); On-site; USD 63,000 - 157,000; Full time

Job summary

IQVIA Inc. seeks a Sr Site Activation Specialist in Durham, NC to manage country-level site activation activities under SOPs and regulations. You will act as SPOC for sites, SAMs, and project teams, guiding feasibility, site ID, startup, and activation processes.

You will review documents, maintain systems, monitor timelines, and provide insights to improve site performance and project delivery. Strong regulatory and clinical research experience are required.

Qualifications

• Bachelor's degree in life sciences or related field.
• 3 years clinical research experience.
• 1 year in a leadership capacity.

Responsibilities

• Serve as Single Point of Contact (SPOC) for investigative sites, SAMs, PM team, and other departments.
• Perform feasibility, site ID, start-up and activation activities per regulations and SOPs.
• Prepare site documents and ensure completeness and accuracy.
• Maintain internal systems and tracking tools with project data.
• Support project timelines and monitor site performance metrics.

Skills

Leadership

Project management

Regulatory knowledge

Education

Bachelor's degree in life sciences or related field

Job description

IQVIA Inc. seeks a Sr Site Activation Specialist in Durham, NC to manage country-level site activation activities under SOPs and regulations. You will act as SPOC for sites, SAMs, and project teams, guiding feasibility, site ID, startup, and activation processes.

You will review documents, maintain systems, monitor timelines, and provide insights to improve site performance and project delivery. Strong regulatory and clinical research experience are required.