Site Activation Specialist in IQVIA

Based in: UkraineMake 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 Site Activation Specialist, you will serve as a Single Point of Contact to 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.You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contractual.Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.You will also 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.Requirements: Bachelor’s Degree in Life Science or related field1 - 3 years’ prior experience in Life Sciences or similar (or equivalent combination of education, training and clinical, healthcare and/or pharma experience)Ability to work independently but also collaborate with othersGood interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsorsAbility to work on multiple projectsKnowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCPJoin IQVIA and let’s create a healthier world together:Exposure across 21 Therapeutic AreasBe part of a global team who operate across 141 locationsExposure across a variety of studies and projectsAccess to new, innovative technologiesWork within a collaborative and vibrant environmentOwn 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 aCzelerate the Development and Commercialization of Innovative Medical Treatments to Help Improve Patient Outcomes and Population Health Worldwide. Learn more at https://jobs.iqvia.com Show More Show LESS Official level Not applied Type of employment Full -time Job responsibilities Information technologies Industry Pharmaceutical production