- 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
Skills
Bachelor’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
Experience with local patients
Certification and Licensure
Professional Membership
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