Senior Clinical Research Associate: Lead On-Site Trials

BairesDev; Quilmes; Hybrid; ARS 92.241.000 - 138.361.000; Vollzeit

Zusammenfassung

IQVIA in Buenos Aires, Argentina seeks a Senior Clinical Research Associate to lead planning, execution, and management of clinical trials. The role emphasizes data integrity, regulatory compliance, and collaboration with diverse teams.

The candidate should have 4+ years of on-site monitoring experience, strong English, and proficiency in CTMS/EDC, with willingness to travel as required. This is a full-time on-site position.

Qualifikationen

• Bachelor's degree in a health care or other scientific discipline.
• 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.

Aufgaben

• 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.
• Comfortably collaborating and communicating with a variety of colleagues and customers.

Kenntnisse

Advanced English

Time management

Communication skills

Independent work

Interpersonal skills

Ausbildung

Bachelor's degree in healthcare or scientific discipline

Tools

CTMS

EDC systems

Jobbeschreibung

IQVIA in Buenos Aires, Argentina seeks a Senior Clinical Research Associate to lead planning, execution, and management of clinical trials. The role emphasizes data integrity, regulatory compliance, and collaboration with diverse teams.

The candidate should have 4+ years of on-site monitoring experience, strong English, and proficiency in CTMS/EDC, with willingness to travel as required. This is a full-time on-site position.