Senior CRA: Global Trials & Compliance, Travel Ready

IQVIA

Buenos Aires

On-site

ARS 138,361,000 - 184,482,000

Full time

4 days ago

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Job summary

IQVIA is seeking a Senior CRA to plan, execute, and manage clinical trials. The role focuses on data integrity, regulatory compliance, and trial success across multiple projects. You will monitor sites, support recruitment planning, and ensure protocol training.

The position requires strong communication and the ability to work independently and with teams in a fast-paced environment. Ideal candidates have a health-care or scientific background, 4+ years of on-site monitoring experience, and

Qualifications

Bachelor's degree in a health care or scientific discipline or equivalent.
Minimum 4 years of on-site monitoring experience.
Proficiency in GCP and ICH guidelines and regulatory requirements.
Strong organizational and time management abilities.
Excellent verbal and written communication and interpersonal skills.
Ability to work independently and as part of a team.
Experience with CTMS and EDC systems.
Willingness to travel as required.

Responsibilities

Perform site initiation, monitoring and close-out visits with documentation.
Support development of a subject recruitment plan.
Train sites on protocol and study procedures and provide ongoing study training.
Evaluate site practices for quality; escalate issues as appropriate.
Track regulatory submissions, recruitment, CRF completion and data queries.
Collaborate with colleagues across functions and external customers.