Clinical Research Coordinator: Impactful Trials

United Research Group LLC; Mar del Plata; On-site; ARS 84,554,000 - 115,301,000; Full time

Job summary

United Research Group LLC is seeking Clinical Research Coordinators at Level I and Level II to coordinate clinical trial activities and support investigators in conducting ethical, compliant, and high-quality clinical research.

Responsibilities and experience expectations will vary according to the assigned coordinator level. The role emphasizes participant screening, consent processes, documentation accuracy, and regulatory compliance in a fast-paced trial environment in Argentina.

Qualifications

• Bachelor's degree in a health-related or scientific field preferred.
• Equivalent relevant experience considered.
• Basic knowledge of clinical research regulations and GCP.
• Strong documentation, communication, and organizational skills.

Responsibilities

• Coordinate protocol-required study activities under investigator oversight.
• Support participant identification, screening, enrollment, and retention.
• Facilitate informed-consent processes as appropriately delegated.
• Schedule and coordinate study visits and protocol-required assessments.
• Maintain accurate source documentation and electronic case report forms.
• Assist with adverse event documentation and timely reporting.
• Support investigational product accountability where assigned and appropriately trained.
• Maintain regulatory documents and delegation records.
• Coordinate with monitors, sponsors, CROs, and study personnel.
• Identify and elevate protocol deviations and data quality concerns.
• Support monitoring visits, audits, and regulatory inspections.

Skills

Documentation

Communication

Organization

Education

Bachelor's degree

Equivalent experience considered

Job description

United Research Group LLC is seeking Clinical Research Coordinators at Level I and Level II to coordinate clinical trial activities and support investigators in conducting ethical, compliant, and high-quality clinical research.

Responsibilities and experience expectations will vary according to the assigned coordinator level. The role emphasizes participant screening, consent processes, documentation accuracy, and regulatory compliance in a fast-paced trial environment in Argentina.