ممرضة باحثة - مكتب التجارب السريرية (ممول بمنحة)
نُشرت يومين تقريبا في الصحة والطب القائمة المختصرةتفاصيل الوظيفة
-
رقم الوظيفة 17729
الوصف الوظيفي
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).
المسؤوليات
- 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.
- يلتزم بمعايير سدرة كما وردت في مدونة قواعد السلوك وسياسات تضارب المصالح
- يلتزم بقيم سدرة ويعززها
نظراً للاحتياجات والفرص المتطورة داخل سدرة، قد يُطلب من شاغل هذه الوظيفة أداء واجبات أخرى حسب التكليف، وقد تختلف علاقات التبعية.
المؤهلات
| ضروري | مفضل | |
| تعليم | Bachelor’s Degree in relevant field (or equivalent) | Post Graduate qualification |
| خبرة |
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 |
| الاعتماد والترخيص |
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 |
| المهارات والقدرات الخاصة بالوظيفة |
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 إتقان استخدام حزمة برامج مايكروسوفت أوفيس إتقان اللغة الإنجليزية كتابةً وتحدثاً |
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 |
المصدر: الموقع الرسمي للوظائف في سدرة للطب. يرجى التقديم مباشرةً لدى جهة العمل.
وظائف أخرى قد تعجبك
-
Medical Doctor Gaza
- الأراضي الفلسطينية المحتلة، فلسطين

