Senior CDMS Data Programmer Consultant — Remote

Veeva; Barcelona; Presencial; EUR 72.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Private health insurance

Flexible paid time off plus local paid

Pension / retirement plan

1% charitable giving program

Descripción de la vacante

Veeva Systems is seeking a Senior Consultant for Vault CDMS who can guide customers through EDC deployments across life sciences trials. This full-time, remote role welcomes candidates from the EU or UK.

You will configure forms, run UAT, integrate data transfers, and mentor teams while upholding regulatory standards and best practices. Travel up to 10% and collaboration with sponsors, CROs, and vendors are included to ensure successful studies.

Formación

• 5+ years of experience with EDC clinical software and end-to-end data management.
• Background in life sciences with pharma/CRO exposure.
• Experience in a customer-facing software services role.
• Willingness to travel up to 10% and possibly international travel.

Responsabilidades

• Act as trusted advisor to customers and sites, ensuring trial designs meet goals and providing training.
• Lead database development and coordinate with sponsor, CRO and other vendors.
• Configure Vault CDMS forms, rules, and data transfers; build SQL-based listings for data cleaning.
• Run UAT and manage feedback, issue resolution, and study acceptance.
• Support requirements gathering and go-live activities; manage regulatory alignment and best practices.

Conocimientos

EDC software

Clinical data management

SQL programming

Life sciences domain

Client-facing

Educación

Degree in Life Sciences, Computer Science, or related field

Herramientas

Vault CDMS

DQS data quality

REST APIs

Descripción del empleo

Veeva Systems is seeking a Senior Consultant for Vault CDMS who can guide customers through EDC deployments across life sciences trials. This full-time, remote role welcomes candidates from the EU or UK.

You will configure forms, run UAT, integrate data transfers, and mentor teams while upholding regulatory standards and best practices. Travel up to 10% and collaboration with sponsors, CROs, and vendors are included to ensure successful studies.