Remote Site Activation Specialist (Argentina)

IQVIA

United States

Remote

USD 52,000 - 70,000

Full time

8 days ago

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Job summary

IQVIA is seeking a Site Activation Specialist for a fully remote position based in Argentina. You will manage country-level SA activities, ensuring regulatory and contractual compliance and coordinating with the SAM and project teams to keep timelines on track.

The role requires a Bachelor’s degree and 2+ years in clinical research, with strong English communication and excellent organizational skills. You’ll contribute to regulatory document readiness and site performance tracking while

Qualifications

Bachelor's degree required.
2+ years of clinical research experience.
Experience with Argentina regulatory activities (ethics committees, ANMAT) optional but preferred.
Good command of English language.
Excellent communication and organizational skills.

Responsibilities

Serve as Single Point of Contact (SPOC) for sites, SAM, PM team and others.
Perform start-up and site activation activities per regulations and SOPs.
Prepare site regulatory documents for completeness and accuracy.
Maintain internal systems and tracking tools with project information.
Provide feedback on site performance metrics to management.
Coordinate project planning, timelines and monitoring measures.
Inform team when regulatory and contractual documents are completed.
Track approval and execution of regulatory, ethics, ICF, and IP release documents.
Provide local expertise during initial and ongoing project timeline planning.
Perform quality control of documents supplied by sites.
May have direct contact with sponsors on specific initiatives.