Senior Clinical Research Associate Jobs In Egypt And Career In Vacancies In Cairo 2016
Job Title Senior Clinical Research Associate
Vacancy Deadline(mm/dd/yy) 8/27/2016
Languages English, Excellent
Country Egypt
City Cairo
Job Category Pharmacy, Health / Medical
Job Type Full Time
Job Level Junior
-Reviews study requirements; conducts pre-study visits and drafts pre-study evaluation reports with QA team. -Acting as the main line of communication with the principle investigator/ CRO. -Oversee the clinical trial progress and ensure that the study is conducted and data and data handled in accordance with the protocol, Good Clinical Practices, applicable ethical and regulatory requirements, guidelines, Standard Operating Procedures and project Gantt chart. -Communicates with investigators and their staff; ensures compliance with terms and conditions reports. -Ensure the compliance of clinical trials protocols & designs with the international guidelines (ICH, FDA, WHO, etc.), project milestones and research proposal to meet international standards. -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. -Ensuring 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). -Verifying 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. -Plan clinical trial materials need and ensure drug accountability is maintained in the site. -Verifying that source data/documents and other trial records are accurate, complete, kept up-to-date, and secured. -Check that the investigator is maintaining the essential documents for the conduct of a Clinical Trial and communicate deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator taking appropriate action designed to prevent recurrence of the detected deviations.
Qualifications Bachelor of Pharmaceutical Science/Medicine/Biology
Gender Any
Car owner Any
Education major Pharmacy
Experience 4 - 5 Years.
Salary (L.E.) Negotiable
Job Contact Email hr_nwe@hotmail.com
Job Title Senior Clinical Research Associate
Vacancy Deadline(mm/dd/yy) 8/27/2016
Languages English, Excellent
Country Egypt
City Cairo
Job Category Pharmacy, Health / Medical
Job Type Full Time
Job Level Junior
-Reviews study requirements; conducts pre-study visits and drafts pre-study evaluation reports with QA team. -Acting as the main line of communication with the principle investigator/ CRO. -Oversee the clinical trial progress and ensure that the study is conducted and data and data handled in accordance with the protocol, Good Clinical Practices, applicable ethical and regulatory requirements, guidelines, Standard Operating Procedures and project Gantt chart. -Communicates with investigators and their staff; ensures compliance with terms and conditions reports. -Ensure the compliance of clinical trials protocols & designs with the international guidelines (ICH, FDA, WHO, etc.), project milestones and research proposal to meet international standards. -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. -Ensuring 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). -Verifying 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. -Plan clinical trial materials need and ensure drug accountability is maintained in the site. -Verifying that source data/documents and other trial records are accurate, complete, kept up-to-date, and secured. -Check that the investigator is maintaining the essential documents for the conduct of a Clinical Trial and communicate deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator taking appropriate action designed to prevent recurrence of the detected deviations.
Qualifications Bachelor of Pharmaceutical Science/Medicine/Biology
Gender Any
Car owner Any
Education major Pharmacy
Experience 4 - 5 Years.
Salary (L.E.) Negotiable
Job Contact Email hr_nwe@hotmail.com
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