ممرض أبحاث سريرية

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).

Responsibilities

• Coordinates the daily job foreseen by the Clinical Research Protocols as agreed with Principal Investigator(s).
• Liaises with Sidra nurses and other external healthcare providers to aid understanding of research principles.
• Obtains consent for research-related interviews and procedures.
• Maintains consent log, detailing reasons for non-consent.
• Performs face-to-face interviews with patients, parents and other subjects serving as controls.
• Assesses the ability of other clinical staff to safely and accurately assist with data collection and entry for research projects.
• Liaises with Medical Records Departments to obtain relevant research data.
• Identifies problems related to patient data and alerts Principle Investigator.
• Organizes, collects, stores, and sends data.
• Organizes, collects and stores biological samples (e.g. blood, saliva, buccal swabs).
• Manages databases of the clinical research protocols assigned to.
• Telephones or visits patients at home to conduct follow-up tests and interviews.
• Supports in the preparation of newsletters and reports.
• Participates in the clinical research protocol creation, amendments, closure, evaluation and reporting.
• 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.

Qualifications

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