Clinical Research Associate (CRA) For Natural Wellness 2016

Clinical Research Associate (CRA) Jobs In Egypt And Career In Natural Wellness  Vacancies In Cairo 2016

Employer Natural Wellness
Job Title Clinical Research Associate (CRA)
Vacancy Deadline(mm/dd/yy) 12/1/2016
 Languages English, Very Good
Country Egypt
City Cairo
Job Category Pharmacy, Research
Job Type Full Time
Job Level Junior
Description Review study requirements; conduct pre-study visits and draft pre-study evaluation reports with QA team. Act as the mainline of communication with the principle investigator and his/her team and the CRO. Ensure that the investigator receives the current Investigators Brochure, all documents, and all trial supplies needed to conduct the trial properly and to comply with the applicable regulatory requirement(s). Verify that the investigator provides all the required reports, notifications, applications, and submissions, and that these documents are accurate, complete, timely, legible, dated, and identify the trial. Check that the investigator is maintaining the essential documents for the conduct of a Clinical Trial along with accuracy and completeness of the CRF entries, source data/documents, and other trial-related records against each other. Oversee the clinical trial progress and ensure that the study is conducted and data is handled in accordance with the protocol, Good Clinical Practice, applicable ethical and regulatory requirements, guidelines, Standard Operating Procedures and project Gantt chart. Control adherence to the protocol, ensuring that data are correctly and completely recorded and reported in the case report form, and confirming that informed consent is being obtained and recorded for all subjects prior to their participation in the trial. Verify that source data/documents and other trial records are accurate, complete, kept up-to-date, and secured. Submit written report to the sponsor after each trial-site visit or trial-related communication (telephone calls, letters, etc), include a summary of what the monitor reviewed and the monitors statements concerning the significant findings/facts, deviations and deficiencies, conclusions, actions taken or to be taken, and/or actions recommended to secure compliance.

Qualifications Bachelor of Pharmaceutical Science/Medicine/Biology Knowledge of GCP principles, Clinical studies procedures and guidelines.
Gender Any
Car owner Any
Education major Pharmacy
Experience 1 - 2 Years.
Salary (L.E.) Negotiable
Comments - CVs without photo will be disregarded. - Please write job title in the subject.
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