Clinical Nutrition Research Assistant

Instituto de Investigación Sanitaria Aragón - IIS Aragón

Zaragoza

On-site

EUR 26,000 - 36,000

Full time

1 hour ago
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Job summary

Instituto de Investigación Sanitaria Aragón - IIS Aragón is seeking a University Mid-Level Research Support Officer – Group C. The role involves assisting in nutritional assessments, supporting interventions for liver disease studies, and managing dietary data under supervision.

You will help with protocol drafting, data transcription in eCRF, and TMF archiving, ensuring compliance with GCP and RD guidelines.

Qualifications

  • Bachelor's degree in nutrition and dietetics required.
  • Six months of experience supporting nutrition/health research projects, preferably in intervention studies with participants.

Responsibilities

  • Assist in nutritional assessment tests and anthropometric measurements under PI supervision.
  • Support in the application and monitoring of nutritional interventions in liver disease studies.
  • Assist with collection and entry of dietary data via 24-hour recalls, frequency questionnaires and food records.
  • Support in draft research protocols for nutrition and hepatology under project manager guidance.
  • Maintain and transfer clinical data in electronic data capture notebooks (eCRF).
  • Review databases for inconsistencies and coordinate with IP or senior staff to resolve queries.
  • Assist TMF management and archiving; provide support during monitoring visits and audits.
  • Facilitate communication between principal investigators, monitors, and the work team; help prepare documentation for CEIm.
  • Support tasks following standardized procedures under PI direction; assist in reports, databases, and preliminary results.

Education

Bachelor's Degree in Human Nutrition and Dietetics

Job description

Instituto de Investigación Sanitaria Aragón - IIS Aragón is seeking a University Mid-Level Research Support Officer – Group C. The role involves assisting in nutritional assessments, supporting interventions for liver disease studies, and managing dietary data under supervision.

You will help with protocol drafting, data transcription in eCRF, and TMF archiving, ensuring compliance with GCP and RD guidelines.

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