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indeed

Research Coordinator

Sidra
QAT
Full-time
Onsite
Discovered 1 months ago
Research coordinationPatient recruitmentSample collectionData collectionDatabase managementInformed consent

Full Job Posting

Overview

The Research Coordinator provides support to the research Investigator's projects.

(S)he is primarily responsible for the coordination between the various stakeholders of the research projects at Sidra and externally, specifically with regard to research subjects recruitment, sample and data collection, liaison with core facilities and recording of databases.

(S)he shall approach patients to collect informed consents and other research protocol-related information and perform other necessary work including IRB protocol processing and translation.

About Us

Sidra Medicine a healthy population is essential to a strong, prosperous society, and throughout 2020, Sidra continued to provide uninterrupted comprehensive specialist healthcare services for children and young people; and exceptional maternity, gynecology, and reproductive medical services for wom

Sidra Medicine represents the vision of Her Highness Sheikha Moza bint Nasser who serves as its Chairperson. This high-tech facility is home to world-class patient care, scientific expertise, and educational resources.

Responsibilities

  • Provide support to the research Investigator's projects.
  • Coordinate between various stakeholders of the research projects at Sidra and externally.
  • Handle research subjects recruitment, sample and data collection.
  • Liaise with core facilities and record databases.
  • Approach patients to collect informed consents and other research protocol-related information.
  • Perform other necessary work including IRB protocol processing and translation.

Requirements

  • Support research Investigator's projects.
  • Coordinate between various stakeholders of research projects at Sidra and externally.
  • Responsible for research subjects recruitment, sample and data collection.
  • Liaison with core facilities and recording of databases.
  • Approach patients to collect informed consents and other research protocol-related information.
  • Perform other necessary work including IRB protocol processing and translation.

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