Site Activation Lead — Clinical Trials

IQVIA Argentina; Indianapolis (IN); On-site; USD 63,000 - 157,000; Full time

Job summary

IQVIA is seeking a country-level Site Activation professional to oversee feasibility, site ID, and activation activities in line with SOPs and regulatory requirements. You will collaborate with the SAM, Project Management, and other departments to ensure timely, accurate documentation and milestone delivery.

You will review project planning, track timelines, and provide local expertise during initial and ongoing planning, while maintaining system accuracy and data integrity across internal tools

Qualifications

• Bachelor's degree in life sciences or related field.
• 3 years clinical research experience, including 1 year in a leadership capacity.
• Equivalent combination of education, training and experience.

Responsibilities

• Serve as Single Point of Contact (SPOC) for investigative sites and project teams under supervision.
• Perform feasibility, site ID, start up and site activation activities per SOPs and regulations.
• Prepare and review site documents for completeness and accuracy.

Skills

Clinical research experience

Leadership experience

Regulatory/compliance understanding

Education

Bachelor's Degree Life science or related field

Job description

IQVIA is seeking a country-level Site Activation professional to oversee feasibility, site ID, and activation activities in line with SOPs and regulatory requirements. You will collaborate with the SAM, Project Management, and other departments to ensure timely, accurate documentation and milestone delivery.

You will review project planning, track timelines, and provide local expertise during initial and ongoing planning, while maintaining system accuracy and data integrity across internal tools