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Clinical Data Analyst - Link Trialbase 🔥

Veeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster. We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed. Our teams develop transformative cloud software, services, consulting, and data to make our customers more efficient and effective in everything they do. Veeva is a work anywhere company. You can work at home, at a customer site, or in an office on any given day. As a Public Benefit Corporation, you will also work for a company focused on making a positive impact on its customers, employees, and communities.The RoleVeeva Link envisions building connected data applications to improve research and patient outcomes. Link TrialBase is a product that optimizes protocol design with reliable, competitive clinical protocol design intelligence. As one of our QA Analysts, you will be the go-to person for all questions about data structure, quality, and insights regarding Link TrialBase. You will interface with product management, data operations, software engineering, data science, quality assurance, and quality control teams. To thrive in your role, you have an academic background or working experience in the life sciences or healthcare industry (focusing on clinical trials). You’ve also acquired initial experience with data analytics, large databases, and complex data sets. Additionally, you are inquisitive, detail-oriented, and highly motivated with a “can do” attitude. You communicate effectively with stakeholders and can deliver high-quality results within a tough timeline. You are comfortable working remotely in an international environment. We care about a great cultural fit. You should enjoy working at speed in multicultural teams. If you are excited about data, Life Sciences, and working for a fast-growing tech company, we are the optimal fit. What You'll Do Own the data flowing from product operations to the Link AppExtract data and provide insights into relational and non-relational databasesIdentify root causes of quality issues in automatic processesAssure data qualityCreate custom reports e.g. for Product Management or Data GovernanceReview and approve training material Requirements University degree in medicine or life sciences 1+ years of working experience in a data analyst or data quality role that requires clinical trial knowledgeIntermediate level of SQL and advanced spreadsheets knowledgeExperience working with large databases and data setsProven ability to manage multiple stakeholdersStrong written and verbal communication skills in English  Nice to Have Experienced in developing manuals, process outlines, and implementation proceduresNoSQL/MongoDBProgramming (Python)Data analysis tools (R, Minitab, Knime)Data visualization tools (Tableau, PowerBI) Perks & Benefits Opportunity to work in a diverse and international workspacePersonal development budgetA significant contribution to the pension fundLife insuranceFitness reimbursement#RemoteGermanyVeeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.

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