Senior Site Activation Expert for Global Clinical Trials

IQVIA; Buenos Aires; On-site; ARS 90,873,000 - 136,310,000; Full time

Job summary

IQVIA is seeking a proactive Site Activation professional to manage country-level activation activities, ensuring compliance with SOPs and project timelines. You will interact with sites, SAMs, and project teams to drive feasibility, site IDs, regulatory reviews, and activation deliverables.

The role involves maintaining documentation quality, monitoring progress, and contributing to process improvements while operating under moderate supervision.

Qualifications

• Bachelor's Degree in Life Sciences or related field is required.
• 3 years of clinical research experience, including leadership exposure.
• Experience with regulatory documents and site activation processes is preferred.

Responsibilities

• Act as SPOC for investigative sites, SAMs, and project teams.
• Perform feasibility, site ID, start up and activation activities ethically and timely.
• Prepare and review site documents for completeness and accuracy.
• Maintain internal systems and databases with project data.
• Provide feedback on site performance metrics to management.

Skills

Clinical research

SOP adherence

Documentation control

Education

Bachelor's Degree in Life Sciences

3 years clinical research experience

Job description

IQVIA is seeking a proactive Site Activation professional to manage country-level activation activities, ensuring compliance with SOPs and project timelines. You will interact with sites, SAMs, and project teams to drive feasibility, site IDs, regulatory reviews, and activation deliverables.

The role involves maintaining documentation quality, monitoring progress, and contributing to process improvements while operating under moderate supervision.