Clinical Reseach Associate I
ICON · Buenos Aires, Argentina
Clinical OperationsFull-timeCompany career page
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Role summary
This Clinical Research Associate I position involves monitoring clinical trials, coordinating study setup activities, and maintaining regulatory compliance at a global clinical research organization. The role requires a science degree, minimum six months of CRA experience, strong English communication skills, and ICH-GCP knowledge. Approximately 60% travel is required.
What they're looking for
- University degree in medicine, science, or equivalent field
- Minimum 6 months clinical research associate experience
- ICH-GCP guidelines knowledge and medical data review expertise
- Fluent written and verbal English communication skills
- Strong interpersonal skills for managing stakeholder queries
- Willingness to travel approximately 60% as required
- Legal right to work in country where role is based
What you'll be doing
- Coordinate study setup and monitoring activities independently with high accuracy
- Complete study status reports and maintain comprehensive study documentation
- Process sponsor-generated queries efficiently and monitor study cost efficiency
- Prepare and review study documentation and feasibility assessments for new proposals
- Build and maintain collaborative relationships with investigators, site staff, and stakeholders
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.