Opportunity overview

United Research Group welcomes qualified medical professionals interested in supporting clinical studies as Sub-Investigators.

Sub-Investigators work under the oversight of the Principal Investigator and perform appropriately delegated study-related responsibilities according to their qualifications, training, and applicable requirements.

This opportunity may involve investigator partnerships rather than traditional employment.

Responsibilities

- Perform protocol-required clinical assessments as appropriately delegated.
- Support participant screening and eligibility evaluation.
- Assist with medical review and participant safety monitoring.
- Participate in informed-consent discussions when qualified and authorized.
- Document study-related clinical findings accurately and promptly.
- Identify and report adverse events and safety concerns.
- Collaborate with the Principal Investigator and study coordination team.
- Maintain required training and delegation documentation.
- Follow approved protocols, ICH-GCP,



and applicable regulatory requirements.
- Support monitoring, audits, and quality reviews as assigned.

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

Proposed Qualifications

- Appropriate medical or clinical professional qualifications for the assigned study responsibilities.
- Active professional licensure where required.
- Relevant clinical experience in the applicable therapeutic area.
- Knowledge of clinical research principles and participant safety.
- Prior Sub-Investigator or clinical research experience preferred.
- Ability to complete GCP and protocol-specific training.
- Strong clinical documentation and communication skills.

Important opportunity information All study activities must remain within the individual's professional scope, documented delegation, training, and applicable regulatory requirements.

Study assignments are not guaranteed.

📌 Sub-Investigator (Mar del Plata)
🏢 United Research Group
📍 Mar del Plata