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 escalate 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.

📌 Clinical Research Coordinator I/II (Mar del Plata)
🏢 United Research Group
📍 Mar del Plata