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Senior Clinical Research Coordinator
3 weeks ago
Responsible for increasing the quality and quantity ofclinical research performed in the Department and therefore promote anatmosphere of serious enquiry among all members of the department especially thejunior staff.
**Essential Responsibilities and Duties**:
1. Maintains an updated log book of all approved clinical research protocols stating the dates of each presentation to be department, initiation, principal investigator, acceptance, if required by other consultants or committees, and publication of the results. Presents regular updates on the ongoing projects and final reports of terminated research.
2. Maintains an updated file of all presentations to local and international meetings, as well as publications by members of the department. Maintains an on-going and updated calendar of future meetings related to malignant diseases and makes it available to all members of the department.
3. Ensures that all clinical materials, which are to be submitted for presentation to meetings or publications comply with the norms of scientific ethics are approved by the department Chairman and Research Advisory Council.
4. Encourages the presentation by the investigator of each new clinical research project, who should present a written proposal distributed to all members of the department prior to the meeting.
5. Performclinical responsibilities within related specialty such as (Nursing,Laboratory, Respiratory, Pharmacy, etc.) as assigned.
6. Ensures the submission of regular reports by the principal investigator of each research project, to be done appropriately and in a timely manner.
7. Maintains and updates the assigned registry, which involves supervision of data gathering and review of patient charts covering neoadjuvant and adjuvant chemotherapy and follows up information on all cancer patients included in the assigned registry, and entering the data into a protocolized questionnaire and inputting into a computer database.
8. Maintains accuracy and completeness of the computer database, as well as generating reports needed by departmental staff.
9. Assists the Director in the evaluation of the clinical research attitude and performance of all members of the department.
**Education**:
Master’s or Bachelor’s Degree in a Clinical field such asNursing, Pharmacy or any field related to health sciences is required.
**Experience Required**:
Four (4) years of Clinical, Healthcare and/or relevantresearch experience with Master’s or six (6) years with Bachelor’s Degree isrequired.
**Other Requirements(Certificates)**:
A successful completion of either a Clinical Research Professional course (offered in house) or any other accredited online course is preferred.
- A certificate of completion of the NIH (_National Institutes of Health)_ web-based training course: “Protecting Human Research Participants” is preferred.
