As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.Your responsibilities will 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 resolution You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.Qualifications:University degree in scientific discipline or healthcareAt least 1 year of on-site monitoring experienceGood knowledge of GCP and clinical research regulatory requirementsGood computer skills including MS OfficeExcellent command of English languageOrganizational, time management and problem-solving skillsAbility to establish and maintain effective working relationships with colleagues, managers, and customers.Flexibility to travel.What you can expect:Working with different customers on global trialsCareer development opportunities for those who are passionate in wanting to grow as part of the organization.Leaders that support flexible work schedules/arrangementExcellent working environment in a stable, international, reputable companyPrograms to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscapeAttractive remuneration package.#LI-HybridIQVIA 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. Learn more at https://jobs.iqvia.comIQVIA 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.