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Sidra Medicine

Research Coordinator

Qatar

  • Mid level

About the role

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.

ESSENTIALPREFERRED

EducationBachelor’s Degree in medicine, natural sciences or other relevant field

Experience

2+ years’ experience in clinical research and/ or clinical research coordination

Experience with patients

Exceptions to the experience requirement may be granted for Qatari nationals (internal and external candidates), with a reduction of up to two (2) years. [For a DHP licensable role, the experience requirements mandated by the Department of Healthcare Professions, along with the defined scope of practice, must be strictly followed.]

Experience with local patients

Job Specific Skills and Abilities

Proven ability to maintain confidentiality

Demonstrated excellent communication skills

Proven electronic documentation, archiving and organizational skills

Proficiency with Microsoft Office suite

Fluency in written and spoken English

Arabic speaker

  • Provides coordination for the investigator’s research projects involving liaison with stakeholders and core facilities.
  • Coordinates recruitment of patients and collects informed consents, assents, questionnaires and related documents.
  • Coordinates samples collection and transportation.
  • Manages the order of reagents/consumables/other items required for the projects.
  • Uses, maintains and organizes a database/folders containing patient information (including secured data and unidentified data, as relevant.
  • Manages the Case Report Forms, according to the different clinical research studies.
  • Adheres to Sidra’s standards as they appear in the Code of Conduct and Conflict of Interest policies
  • Adheres to and promotes Sidra’s Values

In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary.