Clinical Research Associate

ResponsibilitiesThe Clinical Research Associate II or III (CRA II or III) will work in the Clinical Operations with an emphasis placed on ensuring the highest ethical and clinical standards.The CRA II & III are the primary contact person of different stakeholders including but not limited to investigational site staff, study management team, subcontractors involved in studies.Participate in the implementation and monitoring of clinical studies, ensuring quality and reliability of collected data in compliance with regulations and good clinical practices and according to timelines.Actively contributes to maintaining up-to-standard quality of essential documents produced during the different phases of the study from feasibility to close out.The Position is in RiyadhQualifications2 years of experience as a Clinical Research Associate II (CRA II)4 years of experience as a Clinical Research Associate III (CRA III)Bachelor's degree in a health-related fieldWorking knowledge of relevant regulations related to clinical research studies, ICH Guidelines and GCPBusiness proficiency in English & use of Office SuiteExcellent organizational and communication skillsDetail oriented