Senior Clinical Research Associate

Sotalent; Buenos Aires; Remote; ARS 2,009,000 - 2,678,000; Full time

Job summary

Sotalent is seeking a Global Clinical Research Monitor to support regional trials from a home-based setting with approximately 50% travel. The role emphasizes site management, monitoring visits, regulatory compliance, data quality, and close collaboration with clinical research sites and project teams.

The ideal candidate has at least 2 years of hands-on monitoring experience, a healthcare or life sciences degree, and advanced English.

Qualifications

• 2+ years of hands-on clinical trial monitoring experience.
• Bachelor’s degree in healthcare or life sciences.
• Experience working with clinical research sites and study documentation.
• Advanced English proficiency.
• Willingness and ability to travel approximately 50% of the time.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits.
• Support subject recruitment planning and site performance.
• Maintain regular communication with assigned clinical research sites.
• Provide protocol and study-related training to site teams.
• Monitor site practices, data quality, and compliance, escalating issues when required.
• Track regulatory submissions, patient recruitment, CRF completion, and data query resolution.
• Maintain accurate clinical trial documentation.
• Collaborate with internal teams, investigators, sites, and other stakeholders.
• Apply knowledge of applicable clinical research regulations and requirements.

Skills

Clinical monitoring

Regulatory compliance

Data quality

Stakeholder management

Training

Advanced English

Education

Bachelor’s degree in healthcare or life sciences

Job description

Clinical Research / Pharmaceutical industry

• Work arrangement: Home-based
• Travel: Approximately 50%
• Experience: Minimum 2 years of on-site clinical monitoring experience
• Education: Bachelor’s degree in healthcare, life sciences, or another relevant scientific discipline
• Language: Advanced English

Role overview

A global clinical research opportunity supporting clinical trials across the region. The role focuses on site management, monitoring, regulatory compliance, data quality, and maintaining strong communication with clinical research sites and project teams.

Key responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits.
• Support subject recruitment planning and site performance.
• Maintain regular communication with assigned clinical research sites.
• Provide protocol and study-related training to site teams.
• Monitor site practices, data quality, and compliance, escalating issues when required.
• Track regulatory submissions, patient recruitment, CRF completion, and data query resolution.
• Maintain accurate clinical trial documentation.
• Collaborate with internal teams, investigators, sites, and other stakeholders.
• Apply knowledge of applicable clinical research regulations and requirements.

Ideal background

The successful candidate will have:

• At least 2 years of hands-on clinical trial monitoring experience.
• A relevant degree or equivalent combination of education and experience.
• Experience working with clinical research sites and study documentation.
• Strong communication and stakeholder-management skills.
• Good understanding of clinical research regulatory requirements.
• Advanced English proficiency.
• Willingness and ability to travel approximately 50% of the time.
• Current residence in Buenos Aires, Argentina.