Remote CRA II – Growth, Mentoring & Global Projects

IQVIA

Buenos Aires

On-site

ARS 900,000 - 1,500,000

Full time

14 days+

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Job summary

IQVIA LLC is seeking a Clinical Research Associate II for a homebased role in Argentina. The position offers training and mentoring, quarterly performance reviews, and the opportunity to work on global projects with regional travel.

Candidates should be located in Buenos Aires and have 2+ years of on-site monitoring experience with strong English skills. The role involves site visits, recruitment planning support, communication with sites, and monitoring data quality and regulatory progress.

Qualifications

  • Bachelor's degree in a health care or related discipline or educational equivalent.
  • At least 2 years of on-site monitoring experience (Mandatory).
  • Advanced in English (fluency).
  • Availability to travel up to 50%.
  • Located in Buenos Aires, Argentina.

Responsibilities

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation.
  • Supporting the development of a subject recruitment plan.
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites.
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate.
  • Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Skills

On-site monitoring
English proficiency

Education

Bachelor's degree (healthcare or related)

Job description

IQVIA LLC is seeking a Clinical Research Associate II for a homebased role in Argentina. The position offers training and mentoring, quarterly performance reviews, and the opportunity to work on global projects with regional travel.

Candidates should be located in Buenos Aires and have 2+ years of on-site monitoring experience with strong English skills. The role involves site visits, recruitment planning support, communication with sites, and monitoring data quality and regulatory progress.

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