Sidra MedicineResearch Coordinator
AI in this role
Coordinate clinical research projects, patient recruitment, data collection, and protocol management at Sidra.
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.
- 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.
ESSENTIALPREFERREDEducationBachelor’s Degree in medicine, natural sciences or other relevant field Experience2+ 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 patientsJob Specific Skills and AbilitiesProven 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 speakerHow we rate this
Research Coordinator at Sidra Medicine rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
Prepare for this job
A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where clinical research was part of your work. What did you do?
- Tell me about a project where patient recruitment was part of your work. What did you do?
- Tell me about a project where data collection was part of your work. What did you do?
- Tell me about a project where irb protocols was part of your work. What did you do?
- Tell me about a project where medical coordination was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Clinical Research, Patient Recruitment, Data Collection, Irb Protocols, and Medical Coordination. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them — a tool named with nothing behind it rarely survives a human read.
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