Employer MULTISKILLS Recruitment & HR Consultancy
Job Title Clinical Research Associate
Languages Excellent Command Of English
Country Egypt
Job Category Medical Services, Medicine, Pharmacy
Job Type Full Time
Description -Responsible for quality and timely study conduct at assigned sites in accordance with study- specific protocols, good clinical practices, local regulations, and standard operating procedures. The CRA ensures subject safety and the highest possible data quality and integrity. -Perform co-monitoring visits and generate the co-monitoring visit reports for all on-site visits and vendor visits to determine if the trial conduct and clinical monitoring done by Clinical Research Organization ( CRO) is in compliance with the protocol, Standard Operating Procedures (SOPs), International Conference on Harmonization-Good Clinical Practice (ICH-GCP) and all applicable regulations to ensure the rights and well being of patients are protected and that the study data are accurate and reliable. -Review site selection visit, site initiation visit, on-site monitoring visit and close-out visit reports completed by CRO. Identify issues from the review and provide Regional Project Manager (RPM)/CRO for follow up. -Review the Clinical Trial Master File (CTMF) on a regular and ad-hoc interval to ensure all essential documents are in the appropriate files and identify any deficiencies in the documentation before study start, during study conduct and at study close-out to ensure protocol, SOPs and regulatory compliance.
Qualifications -Minimum 1 to 2 years of Experience as a Clinical Research Associate -High communication skills internally with other departments and externally with doctors & hospitals. -High Customer Services -High Presentation Skill
Gender Any
Experience 1 - 2 Years.
Salary (L.E.) Negotiable
Job Contact Info. info@multi-skills.com
Job Title Clinical Research Associate
Languages Excellent Command Of English
Country Egypt
Job Category Medical Services, Medicine, Pharmacy
Job Type Full Time
Description -Responsible for quality and timely study conduct at assigned sites in accordance with study- specific protocols, good clinical practices, local regulations, and standard operating procedures. The CRA ensures subject safety and the highest possible data quality and integrity. -Perform co-monitoring visits and generate the co-monitoring visit reports for all on-site visits and vendor visits to determine if the trial conduct and clinical monitoring done by Clinical Research Organization ( CRO) is in compliance with the protocol, Standard Operating Procedures (SOPs), International Conference on Harmonization-Good Clinical Practice (ICH-GCP) and all applicable regulations to ensure the rights and well being of patients are protected and that the study data are accurate and reliable. -Review site selection visit, site initiation visit, on-site monitoring visit and close-out visit reports completed by CRO. Identify issues from the review and provide Regional Project Manager (RPM)/CRO for follow up. -Review the Clinical Trial Master File (CTMF) on a regular and ad-hoc interval to ensure all essential documents are in the appropriate files and identify any deficiencies in the documentation before study start, during study conduct and at study close-out to ensure protocol, SOPs and regulatory compliance.
Qualifications -Minimum 1 to 2 years of Experience as a Clinical Research Associate -High communication skills internally with other departments and externally with doctors & hospitals. -High Customer Services -High Presentation Skill
Gender Any
Experience 1 - 2 Years.
Salary (L.E.) Negotiable
Job Contact Info. info@multi-skills.com
