Americas Site Activation Specialist

IQVIA

Buenos Aires

On-site

ARS 1,200,000 - 2,400,000

Full time

14 days+

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Job summary

IQVIA is a leading global provider of clinical research services and healthcare insights. The role involves feasibility, site activation, and regulatory support across studies, serving as the main point of contact for investigative sites while coordinating with the SAM and PM teams.

Based in Argentina or nearby regions, English proficiency is required to collaborate with US teams. Ideal candidates have life sciences background and 1–3 years of clinical research experience, with strong document

Qualifications

Bachelor’s Degree Life sciences or a related field required.
1–3 years’ clinical research supporting site activation/regulatory tasks.
Advanced level of English.
Based in Argentina or Brazil.

Responsibilities

Serve as SPOC to perform feasibility, site activation and some maintenance activities in assigned studies.
Review documents for completeness, consistency and accuracy under guidance of senior staff.
Prepare and review site documents for completeness and accuracy.
Inform team members of completion of regulatory and other documents for sites.
Distribute completed documents to sites and project team members.
Update internal systems, databases, tracking tools, timelines and project plans with accurate information.
Review and track progress, approval and execution of regulatory documents (ICF, CDA, ethics, IP release).