Senior CRA - Cardiology Clinical Trials

Diagnosticomaipu; Quilmes; On-site; ARS 92,724,000 - 139,086,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Research Associate in Buenos Aires, Argentina, for full-time on-site monitoring of clinical trials. The role focuses on ensuring data integrity, regulatory compliance, and effective site management across projects.

Strong English, documentation, and CTMS/EDC proficiency are required. The candidate will perform site visits, support recruitment planning, and maintain protocol training at sites, while ensuring quality across trial activities.

Qualifications

• Bachelor's degree in health care or other scientific discipline or equivalent
• At least 4 years of on-site monitoring experience
• Advanced in English
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements
• Strong organizational and time management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Proficiency in CTMS and EDC systems
• Willingness to travel as required

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
• Comfortable collaborating and communicating with a variety of colleagues and customers, with knowledge of applicable regulatory requirements

Skills

Site monitoring

English proficiency

Communication skills

Organizational/time management

Independent work / teamwork

Education

Bachelor's degree in health care or scientific field

Tools

CTMS

EDC systems

Job description

IQVIA is seeking a Senior Clinical Research Associate in Buenos Aires, Argentina, for full-time on-site monitoring of clinical trials. The role focuses on ensuring data integrity, regulatory compliance, and effective site management across projects.

Strong English, documentation, and CTMS/EDC proficiency are required. The candidate will perform site visits, support recruitment planning, and maintain protocol training at sites, while ensuring quality across trial activities.