وصف الوظيفة
Role Overview
Research Coordinator at Sidra Medicine. The role is based at Sidra Medicine's facility in Qatar.
Company Overview
Sidra Medicine is a high-tech facility providing world-class patient care, scientific expertise, and educational resources. The organization delivers comprehensive specialist healthcare services for children and young people, and exceptional maternity, gynecology, and reproductive medical services for women.
Role Purpose
The Research Coordinator provides comprehensive support to research Investigators' projects, serving as the primary liaison between internal stakeholders, core facilities, and external partners. The role manages all aspects of research subject recruitment, informed consent collection, sample and data management, and protocol compliance to ensure smooth execution of research initiatives.
Key Responsibilities
Stakeholder Coordination
- Provide coordination for the Investigator's research projects involving liaison with stakeholders and core facilities.
- Liaison with core facilities as required by research projects.
Patient Recruitment & Consent
- Coordinate recruitment of patients for research studies.
- Approach patients to collect informed consents and assents.
- Collect questionnaires and related research protocol documentation from research subjects.
Sample & Data Management
- Coordinate samples collection and transportation.
- Manage and maintain databases and folders containing patient information, including secured data and unidentified data as relevant.
- Manage Case Report Forms according to different clinical research studies.
- Perform electronic documentation, archiving, and organizational work.
Operations & Resources
- Manage the order of reagents, consumables, and other items required for research projects.
- Perform IRB protocol processing and translation as necessary.
Compliance & Standards
- Adhere to Sidra's standards as they appear in the Code of Conduct and Conflict of Interest policies.
- Adhere to and promote Sidra's Values.
Additional Duties
- Perform other duties as assigned in view of evolving needs and opportunities within Sidra.
Qualifications & Experience
- Bachelor's Degree in medicine, natural sciences, or other relevant field.
- Minimum 2+ years' experience in clinical research and/or clinical research coordination.
- Experience working with patients.
- Experience with local patients.
- Exceptions to the experience requirement may be granted for Qatari nationals (internal and external candidates), with a reduction of up to two years.
Skills & Competencies
- 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.
Additional Information
- Reporting relationships may vary in view of evolving needs and opportunities within Sidra.