• 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