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Salary: HUF 18,000,000 - 33,000,000 / annual
Veeva Systems is a public benefit corporation and industry-leading SaaS provider in life sciences, helping companies bring therapies to patients faster. The company surpassed $3B in revenue last fiscal year and operates as a Work Anywhere organization supporting flexible work arrangements.
The Role
Veeva's Vault Clinical Data Management System (CDMS) is transforming how life sciences companies manage clinical trial data by consolidating EDC, coding, and Data Quality System (DQS) functionality. The Migration Team focuses on migrating customers from legacy systems—such as Medidata Rave and Oracle InForm—into Vault CDMS. You will serve as a Senior Migration Consultant, acting as a trusted technical lead and customer-facing expert partnering directly with Sponsors and CROs throughout active migration programs.
Key Responsibilities
- Partner directly with Sponsors and CROs to interpret legacy clinical database structures, protocol specifications, and data mapping requirements, applying Veeva migration best practices
- Perform data transformation, mapping, and script validation on large, complex clinical datasets extracted from legacy platforms (e.g., Medidata Rave, Oracle InForm)
- Lead end-to-end data migration delivery across complex, active clinical trials per project plans, coordinating with cross-functional technical teams
- Develop and configure validation scripts and custom SQL-based listings to ensure data integrity, auditability, and cleanliness during ingestion into Veeva DQS and Vault CDMS
- Provide feedback to product teams based on real-world customer migration challenges, data volume bottlenecks, and client requirements
- Contribute to reusable migration tools, data mapping templates, and automation initiatives while mentoring junior team members
- Travel up to 10%, potentially including international travel
Requirements
- 5+ years of experience with EDC clinical software, covering end-to-end data management (database design, data collection, data analysis, query resolution, datasets, statistical reporting)
- Solid understanding of clinical trial processes, particularly around data collection and review
- Programming experience in SAS, R, Python, or SQL, with ability to pick up new SQL-based languages
- Background in life sciences industry (pharma, biotech, medical device, CRO, or academic/public health), with experience across project assessment, planning, development, training, and implementation
- Experience in customer-facing roles, ideally within software professional services or consulting
- Ability to work independently and collaboratively in fast-paced, dynamic environments while meeting project timelines
- Strong verbal and written communication, interpersonal, and presentation skills
Nice to Have
- Knowledge of DBT
- Familiarity with data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM)
- Experience with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, or similar clinical technologies
- Experience integrating or programming with REST-based APIs
- Experience translating clinical protocols into software specifications
- Experience with Veeva applications
- Location near major life sciences hub
- Degree in Life Sciences, Computer Science, or related field
