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IQVIA

Registered Dietitian - Clinical Research Support - Remote - Part-Time

6w

IQVIA

Buenos Aires, AR · Part-time

About this role

IQVIA is seeking experienced and registered Dietitians to join our team for an international clinical research project in the metabolic disease area. This freelance, part-time role offers the flexibility to work remotely from anywhere in Argentina, specifically supporting patients in the Province of Tucuman.

In this role, you will conduct comprehensive nutritional assessments and provide ongoing counseling and motivational support to study participants. All meetings and consultations are conducted online via telehealth, allowing you to monitor participant progress and outcomes throughout the study period from your home.

You will collaborate closely with the clinical research team to ensure adherence to study protocols, maintaining accurate and confidential documentation in compliance with regulatory standards. As part of a global leader in healthcare innovation, you will participate in virtual team meetings and training sessions, contributing to a collaborative and forward-thinking environment.

This position offers a unique opportunity to contribute to a high-impact international clinical study while advancing your career in clinical research. You will gain exposure to global research standards and work with an international team, all from the comfort of your home in Argentina.

Requirements

  • Certified and Registered Dietitian in the Province of Tucuman, Argentina
  • Fluent in English; additional language skills are a plus
  • Strong interpersonal and communication skills
  • Ability to work independently and in a structured manner
  • Clinical experience preferred
  • Proficient with digital tools and telehealth platforms

Responsibilities

  • Conduct comprehensive nutritional assessments for study participants
  • Provide ongoing counseling and motivational support to participants
  • Monitor participant progress and outcomes throughout the study period
  • Conduct all meetings and consultations with participants online via telehealth
  • Collaborate with the clinical research team to ensure adherence to study protocols
  • Maintain accurate and confidential documentation in compliance with regulatory standards
  • Participate in virtual team meetings and training sessions

Benefits

  • Opportunity to contribute to a high-impact international clinical study
  • Remote work and collaboration with an international team
  • All participant interactions and monitoring are conducted online
  • Professional development and exposure to global research standards