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Salary: HUF 18,000,000 - 33,000,000 / annual
Veeva Systems is seeking a Senior Migration Consultant to lead clinical data migration initiatives for its Vault Clinical Data Management System (CDMS). This is a customer-facing technical role focused on migrating life sciences organizations from legacy systems such as Medidata Rave and Oracle InForm into Vault CDMS.
In this position, you will partner directly with Sponsors and CROs to interpret legacy clinical database structures, protocol specifications, and data mapping requirements while applying Veeva migration best practices. You will perform data transformation, mapping, and script validation on large, complex clinical datasets extracted from legacy platforms. Your responsibilities include leading end-to-end data migration delivery across complex, active clinical trials per project plans, coordinating with cross-functional technical teams, and developing validation scripts and custom SQL-based listings to ensure data integrity and auditability during ingestion into Veeva DQS and Vault CDMS.
You will also provide feedback to product teams based on real-world customer migration challenges and data volume bottlenecks, contribute to reusable migration tools and data mapping templates, and mentor junior team members throughout the migration lifecycle. This role requires strong technical expertise in clinical data management combined with excellent customer-facing communication and the ability to work independently in a fast-paced environment.
Veeva is a public benefit corporation and mission-driven organization pioneering industry cloud solutions for life sciences. The company surpassed $3B in revenue in its last fiscal year and operates as a Work Anywhere company supporting flexible work arrangements.
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 role, ideally within software professional services or consulting
- Ability to work independently and collaboratively in fast-paced, dynamic environment while meeting project timelines
- Strong verbal and written communication, interpersonal, and presentation skills
- Willingness to travel up to 10%, potentially including international travel
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
