Clinical Research Coordinator I/II

United Research Group LLC; Mar del Plata; Presencial; ARS 84.554.000 - 115.301.000; Jornada completa

Descripción de la vacante

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.

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Documentation

Communication

Organization

Educación

Bachelor's degree

Equivalent experience considered

Descripción del empleo

Position overview

United Research Group 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.

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.

The qualifications below are proposed recruitment criteria pending final URG approval.

Proposed Qualifications — Clinical Research Coordinator I

• Bachelor's degree in a health-related or scientific field preferred; equivalent relevant experience considered.
• Entry-level to approximately 2 years of clinical research or related healthcare experience preferred.
• Basic knowledge of clinical research regulations and GCP.
• Strong documentation, communication, and organizational skills.

Proposed Qualifications — Clinical Research Coordinator II

• Bachelor's degree or equivalent relevant experience preferred.
• Approximately 2-4 years of clinical research coordination experience preferred.
• Demonstrated experience managing clinical trial activities and study documentation.
• Working knowledge of ICH-GCP, informed consent, adverse event reporting, and EDC systems.
• Ability to manage competing study priorities with appropriate investigator oversight.