Senior Site Activation Coordinator - Exclusive for People With Disabilities job opportunity at IQVIA Holdings, Inc..

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IQVIA Holdings, Inc. Senior Site Activation Coordinator - Exclusive for People With Disabilities
Experience: 2-years
Pattern: full-time
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degreeAssociate
loacation São Paulo, Brazil, Brazil
loacation São Paulo, Bra..........Brazil

This is a talent pool for people with disabilities . If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs Important: Please, submit your CV and laudo when applying. Make an impact on patient health IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available. Job Overview: As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities. These activities will be in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. You will perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions, working closely with the Site Activation Manager, Project Management team, and other departments as necessary. Coupled with reviewing documents for completeness, consistency, and accuracy, under guidance of senior staff, you will prepare site documents, review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents. You will also support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information. Requirements: Bachelor’s Degree in Life Science or related field Minimum 2 years’ work experience; 1+ years in healthcare handling regulatory tasks in a clinical research environment Good interpersonal, communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors Ability to work on multiple projects Join IQVIA and let’s create a healthier world together: Exposure across 21 Therapeutic Areas Be part of a global team who operate across 141 locations Exposure across a variety of studies and projects Access to new, innovative technologies Work within a collaborative and vibrant environment Own your career! Unleash your potential! It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward. IQVIA 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.com

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