Clinical Research Associate II: Monitor Trials & Compliance

ThermoFisher Scientific; Buenos Aires; On-site; ARS 1,800,000 - 2,400,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join our global team in Argentina. You will perform and coordinate clinical monitoring and site management, conduct remote or on-site visits, and ensure adherence to protocol, ICH-GCP guidelines, and regulatory requirements.

Strong documentation and communication skills are essential for successful trial oversight. The role involves interactions with multiple sponsors, maintaining audit readiness, and collaborating

Qualifications

• Bachelor's degree in a life sciences related field or Nursing certification.
• Experience performing clinical monitoring and site management activities is valued.
• Proven ability to work with ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Perform and coordinate all aspects of clinical monitoring and site management.
• Conduct remote or on-site visits to assess protocol compliance and manage documentation.
• Develop and follow up on monitoring plans, reports and issue resolutions.

Skills

Clinical monitoring

Regulatory ICH-GCP

Documentation

Communication

Time management

Education

Bachelor's in life sciences

Nursing certification

Tools

Microsoft Office

Job description

Thermo Fisher Scientific is seeking a Clinical Research Associate (Level II) to join our global team in Argentina. You will perform and coordinate clinical monitoring and site management, conduct remote or on-site visits, and ensure adherence to protocol, ICH-GCP guidelines, and regulatory requirements.

Strong documentation and communication skills are essential for successful trial oversight. The role involves interactions with multiple sponsors, maintaining audit readiness, and collaborating