Clinical Research Associate Jobs In Egypt And Career In Vacancies In Cairo 2016
Job Title Clinical Research Associate
Languages -Excellent English Spoken/Written.
Languages English, Excellent
Country Egypt
City Cairo
Job Category Medicine, Pharmacy, Health / Medical
Job Type Full Time
Job Level Senior
1. Follow up on clinical trials conducted for the company products for phase I ( pharmacokinetics ) , Phase II and Phase III 2. Oversee the trail progress and ensure that the study is conducted and data and data handled in accordance with the protocol, Good Clinical Practices, and applicable ethical and regulatory requirements. 3. Controlling adherence to the protocol, ensuring that data are correctly and completely recorded and reported, and confirming that informed consent is being obtained and recorded for all subjects prior to their participation in the trial. 4. Acting as the main line of communication between the sponsor and the investigator. 5. 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). 6. Verifying that the investigator and the investigators trial staff are performing the specified trial functions, in accordance with the protocol and any other written agreement between the sponsor and the investigator/institution, and have not delegated these functions to unauthorized individuals. 7. Verifying that source data/documents and other trial records are accurate, complete, kept up-to-date, and maintained. 8. 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. 9. Checking the accuracy and completeness of the CRF (Case Report Form) entries, source data/documents, and other trial-related records against each other. 10. Determining whether the investigator is maintaining the essential documents for the Conduct of a Clinical Trial.
Qualifications -MBBCh /Pharmacist / Vet. -Knowledge of GCP principles, Clinical studies procedures and guidelines. -5 years experience, MSc is beneficial. -Excellent English Spoken/Written. -Excellent salary & fringe benefits.
Gender Any
Car owner Any
Education major Medicine
Experience 4 - 5 Years.
Salary (L.E.) Negotiable
Comments A 8Multinational 8Nutraceutical 8company (Based 8in 8Nasr 8City)
Job Contact Email Hr_nwe@hotmail.com
Job Title Clinical Research Associate
Languages -Excellent English Spoken/Written.
Languages English, Excellent
Country Egypt
City Cairo
Job Category Medicine, Pharmacy, Health / Medical
Job Type Full Time
Job Level Senior
1. Follow up on clinical trials conducted for the company products for phase I ( pharmacokinetics ) , Phase II and Phase III 2. Oversee the trail progress and ensure that the study is conducted and data and data handled in accordance with the protocol, Good Clinical Practices, and applicable ethical and regulatory requirements. 3. Controlling adherence to the protocol, ensuring that data are correctly and completely recorded and reported, and confirming that informed consent is being obtained and recorded for all subjects prior to their participation in the trial. 4. Acting as the main line of communication between the sponsor and the investigator. 5. 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). 6. Verifying that the investigator and the investigators trial staff are performing the specified trial functions, in accordance with the protocol and any other written agreement between the sponsor and the investigator/institution, and have not delegated these functions to unauthorized individuals. 7. Verifying that source data/documents and other trial records are accurate, complete, kept up-to-date, and maintained. 8. 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. 9. Checking the accuracy and completeness of the CRF (Case Report Form) entries, source data/documents, and other trial-related records against each other. 10. Determining whether the investigator is maintaining the essential documents for the Conduct of a Clinical Trial.
Qualifications -MBBCh /Pharmacist / Vet. -Knowledge of GCP principles, Clinical studies procedures and guidelines. -5 years experience, MSc is beneficial. -Excellent English Spoken/Written. -Excellent salary & fringe benefits.
Gender Any
Car owner Any
Education major Medicine
Experience 4 - 5 Years.
Salary (L.E.) Negotiable
Comments A 8Multinational 8Nutraceutical 8company (Based 8in 8Nasr 8City)
Job Contact Email Hr_nwe@hotmail.com
