The Research Nurse works within the Clinical Trial Office in the Advanced Cell Therapy Core to coordinate clinical investigators and assist scientists in conducting clinical research.
(S)he is primarily responsible for the enrollment of human subjects, for biological sample and data collection, and delivers these to the research laboratories involved of the biological sample and data processing. (S)he ensures biological sample and data collection and entry/storage is conducted within stringent guidelines and assists the clinical investigators in preparing or amending study protocols for review and approval by the respective Institutional Review Board(s).
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.
| ESSENTIAL | PREFERRED | |
| Education | Bachelor’s Degree in relevant field (or equivalent) | Post Graduate qualification |
| Experience | 3+ years’ experience in clinical research Broad clinical practice experience
| Experience of clinical research in feto-maternal health and/or child health Experience with Clinical Disease Registries |
| Certification and Licensure | Registered by relevant regulatory body (or equivalent) in country of origin QCHP licensing available or obtainable within 6 months Training and Certificate of Good Clinical Practice | The Society of Clinical Research Associates Certificate |
| Job Specific Skills and Abilities | Demonstrated knowledge of patient-interviewing Demonstrated knowledge of data-collection Demonstrated ability in supporting clinical research projects Demonstrated knowledge and application of good clinical practice Computing/IT proficiency Word processing proficiency Proficiency with Microsoft Office suite Fluency in written and spoken English | Knowledge of Arabic culture in the Arabian Gulf Experience with Database and Statistics Software Fluency in written and spoken Arabic Knowledge of regulatory issues related to the conduct of research |
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