Remote In-House Clinical Research Associate I/II

Worldwide Clinical Trials Holdings, Inc.; Argentina; Remote; ARS 1,800,000 - 3,000,000; Full time

Job summary

Worldwide Clinical Trials is seeking an In-House Clinical Research Associate for a remote role open to candidates in Argentina or Brazil. You will collaborate with global teams to support site management, monitoring, and study lifecycle activities, ensuring alignment with GCP and regulatory requirements.

The role emphasizes site documentation, data review in EDC systems, and coordinating with Clinical Trial Managers and field CRAs to deliver study milestones on schedule.

Qualifications

• A four-year college curriculum in medical/biological/health sciences preferred; or two-year plus CAC/experience.
• Knowledge of FDA/EU regulations, ICH guidelines, and local regulatory requirements.
• Strong written and verbal communication skills for cross-functional teams.
• Organizational skills with the ability to manage multiple activities efficiently.
• Experience with electronic data capture (EDC) and trial documentation fundamentals.

Responsibilities

• Support site management activities across the study lifecycle, including initiation, monitoring, and close-out.
• Coordinate with Trial Managers and CRAs to keep study activities on track.
• Review trial site documentation and assist TMF filing and ISF maintenance.
• Review EDC records for quality and compliance; resolve data queries with sites.
• Prepare CRAs for site visits and track action items, deviations, and training.

Skills

English

Spanish

Portuguese

Communication

Regulatory knowledge

Education

Bachelor degree or equivalent in life sciences

Clinical research experience

Tools

EDC systems

IVRS

Microsoft Office

Job description

Worldwide Clinical Trials is seeking an In-House Clinical Research Associate for a remote role open to candidates in Argentina or Brazil. You will collaborate with global teams to support site management, monitoring, and study lifecycle activities, ensuring alignment with GCP and regulatory requirements.

The role emphasizes site documentation, data review in EDC systems, and coordinating with Clinical Trial Managers and field CRAs to deliver study milestones on schedule.