Experienced Clinical Research Associate - Multi-Sponsored Model

Clinical Research Associate OpportunityIf you want to do your next step as a CRA, this is your chance! You'll have training and development to plan and progress your career in the direction you choose. And you won't do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. While projects vary, your typical responsibilities might include: Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices – escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionYou will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: A Bachelor's degree in a health care or other scientific discipline or educational equivalentAt least 1,5 - 2 years of on-site monitoring experienceFluent in Arabic and English languageGood written and verbal communication skills including good command of English languageRequires frequent travel to sitesFlexible about location, but location must have good connectivity to travelHomebasedIf you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team. Connect to great opportunityTMIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.