Senior Business Analyst in Bucuresti

Who are we?We are the creators of ClinSpark - the world’s first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (now known as the ‘IQVIA Clinical eSource Platform) improves the speed, quality, and transparency of clinical research. Our product platform supports a large and growing set of device integrations, enabling data collected from trial subjects, both onsite and remote, to be immediately available for review by study teams and the sponsor.We’re part of the group within – a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. We are distributed team, working in a remote capacity. This approach offers all of us a great deal of freedom and flexibility. We value a healthy work-life balance. Family matters to us.Working in our team can be challenging, it is certainly never boring, but above all, it is incredibly rewarding.Learn more about our product: About youYou find joy in helping your customers (biopharmaceutical, clinical research organizations) who are doing important work.Creative thinker who strives to solve The Larger Problem when presented with a specific issue.Hungry to learn, self motivated, persistent, and detail oriented.Strong technical aptitude and Business Analysis experience as a member of a software development team.You should love being part of cross-functional teams who build and deliver solutions, while applying your creativity and focus.You have experience working directly with technical partners, customers, stakeholder groups, and end users to understand and translate business needs into software requirements.About the roleYou’ll be part of a geographically diverse, highly professional team comprised of domain experts, former clinical research practitioners, product owners, software testers, project managers, and engineers tackling all aspects of our business and operations.As a Senior Business Analyst, you will lead the efforts to gather, analyze, define, document, and validate software requirements. This will include key functions of the core web application, connected devices, data visualization, and reporting capabilities. All of these efforts will be an essential part of the IQVIA Connected Devices Product Delivery team, and supporting the overall growth and capabilities of the IQVIA Clinical eSource Platform.This role will help drive effective planning, reporting, and analysis to internal functions.You will create and contribute to technical documentation of the product in support of SDLC, including software design documents, functional specifications, and change requests. Occasionally, you will also need to create diagrams and other visual assets to depict capabilities and workflows.You must be able to work at the highest technical level of most phases of systems analysis, while considering the implications of the application of technology to the current and future business environment.This position is fully remote. Candidates in European timezones will be at an advantage.QUALIFICATIONSMust Have Minimum five (5) years of related systems or business analysis experienceKnowledge of software development processes and best practicesAbility to work independently and in a remote team environmentStrong technical skills with experience working within software development teamsExperience with Software Development Life Cycle (SDLC) methodologies, including verification and validation activitiesExperience with BDD methodologies and requirement definitionStrong analytical and problem solving skillsExcellent communication and interpersonal skillsDetail-oriented with excellent time management and organizational skillsDemonstrated ability to understand client requirements as well as underlying infrastructure applications, systems and processes to enable execution of those skillsNice To Have Bachelor's Degree Computer Science or Business Administration, or equivalent experienceExperience with Atlassian systems (Jira and Confluence)Knowledge of business-wide applications (e.g. third party software and internal operational applications, etc.) or IQVIA client facing applications and productsKnowledge of Phase I-IV clinical trial operations and workflowsExpertise pertaining to clinical trial management softwareKnowledge of applicable clinical research, regulatory and other requirements; i.e., Good Clinical Practice, HIPAA, GDPR, EMA, GAMP5, FDA 21 CFR Part 11IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at


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