Senior Clinical Research Associate

Atlas Search; Argentina; On-site; ARS 1,000,000 - 1,400,000; Full time

Job summary

Atlas Search is seeking a Senior Clinical Research Associate in Argentina to lead oversight of assigned clinical sites across Phase I–IV studies. You will ensure trials run per protocol, ICH-GCP, SOPs, and regulatory requirements, from site start-up to close-out.

You will monitor site performance, coordinate visits, SDV activities, and maintain strong investigator relationships to support timely study milestones.

Qualifications

• MUST be bilingual including 100% fluent in English
• Bachelor's Degree in Life Science discipline required
• Bachelor's Degree in Nursing or RN a plus
• Minimum 3 years of direct site monitoring experience required
• Detailed understanding of clinical site monitoring and overall drug development

Responsibilities

• Oversee start-up, monitoring, and execution of Phase I–IV studies at assigned sites
• Monitor compliance with ICH-GCP, SOPs, study protocols, and local regulations
• Serve as primary contact for sites throughout the study lifecycle
• Coordinate monitoring schedules and ensure timely visits, data entry, and milestones
• Perform routine monitoring including SDV to ensure data integrity and protocol adherence
• Build and maintain strong relationships with investigators and site personnel

Skills

Fluent English

Education

Bachelor's Degree in Life Science

Bachelor's Degree in Nursing or RN

Job description

We are partnered with a growing company that is seeking a Senior Clinical Research Associate. The Senior Clinical Research Associate is responsible for the overall management and oversight of assigned clinical trial sites, including site identification, feasibility assessments, pre-study evaluations, study start-up, site initiation, patient recruitment, site monitoring, close-out activities, inspection readiness, and local regulatory and IRB/EC submissions. This role ensures clinical studies are conducted in accordance with study protocols, Standard Operating Procedures (SOPs), ICH-GCP guidelines, and all applicable regulatory requirements while supporting the successful execution of clinical programs.

Responsibilities:

• Oversee the successful start-up, monitoring, and execution of Phase I-IV clinical studies at assigned investigative sites.
• Conduct clinical site management and monitoring activities in compliance with ICH-GCP guidelines, Standard Operating Procedures (SOPs), study protocols, applicable study plans, local regulations, and internal working procedures.
• Serve as the primary point of contact for assigned clinical sites throughout the entire study lifecycle, from site start-up through close-out.
• Coordinate monitoring schedules and ensure timely completion of site visits, data entry, and study milestones at assigned sites.
• Perform routine monitoring activities, including source data verification (SDV), to ensure data integrity, protocol compliance, and adherence to established study timelines.
• Build, maintain, and strengthen relationships with investigators and site personnel to promote effective communication, site engagement, and successful study execution.

Qualifications:

• MUST be bilingual including 100% fluent in English
• Bachelor's Degree in a Life Science discipline required
• Bachelor's Degree in Nursing or RN a plus
• Minimum 3 years of direct site monitoring experience required
• Detailed understanding of all aspects of clinical site monitoring and understanding of overall drug development.