Senior Site Activation Lead for Clinical Trials

IQVIA Argentina; Wayne (NJ); On-site; USD 63,000 - 157,000; Full time

Job summary

IQVIA is seeking a Site Activation professional to execute country-level SA activities in accordance with applicable regulations, SOPs, and project requirements. You will work under moderate supervision, supporting feasibility, site identification, startup, and activation processes.

This role emphasizes accurate site documentation, data maintenance, and timely communication with sponsors and internal teams. Leadership experience is valued for guiding timelines and quality control across sites.

Qualifications

• Bachelor's degree in life science or related field.
• 3 years of clinical research or other relevant experience.
• 3 years clinical research experience, including 1 year experience in a leadership capacity.

Responsibilities

• Serve as Single Point of Contact (SPOC) in assigned studies for sites, SAM, PM team, and other departments; ensure SOPs and timelines are followed.
• Perform feasibility, site ID, start up and site activation activities per regulations and SOPs; distribute documents to sites and team.
• Prepare site documents, reviewing for completeness and accuracy.
• Maintain internal systems, databases and tracking tools with project-specific information.
• Review and provide feedback on site performance metrics and project timelines.

Skills

Clinical research experience

Leadership experience

Education

Bachelor's Degree Life science or related field

Job description

IQVIA is seeking a Site Activation professional to execute country-level SA activities in accordance with applicable regulations, SOPs, and project requirements. You will work under moderate supervision, supporting feasibility, site identification, startup, and activation processes.

This role emphasizes accurate site documentation, data maintenance, and timely communication with sponsors and internal teams. Leadership experience is valued for guiding timelines and quality control across sites.