Senior Clinical Data Programming Consultant (Remote)

Veeva; Greater London; On-site; GBP 95,000 - 125,000; Full time

Benefits offered by this job

Private health insurance

Flexible paid time off plus local PH

Pension / retirement plan

1% charitable giving program

Job summary

Veeva Systems is seeking a Senior Consultant with life sciences software programming experience to help customers maximize EDC on Vault CDMS. This full-time, remote-from-EU/UK role combines advisory and hands-on development, including data transfers, SQL listings, and UAT support.

You will work with sponsors, CROs, and data providers, applying Veeva best practices, and travel up to 10% as needed. A life sciences or CS degree is preferred with 5+ years in EDC and REST API experience.

Qualifications

• 5+ years in end-to-end data management for clinical software (EDC).
• Solid understanding of clinical trial processes and data flow.
• Programming experience in SAS, R, JSON, Python or SQL, with ability to learn new SQL-based languages.
• Life sciences background across pharma/biotech/CRO and related areas.
• Customer-facing experience in software professional services or consulting.
• Ability to work independently and collaboratively in fast-paced projects.
• Strong verbal and written communication and presentation skills.
• Willingness to travel up to 10%, including international travel.
• Familiarity with GCDMP, CDISC, SDTMIG, CDASH, ADaM standards.
• Experience with system integrators for IVRS, eSource, CTMS, eTMF, etc.
• Experience integrating or programming with REST-based APIs.
• Experience translating clinical protocols into software specifications and tech docs.
• Experience with Veeva applications.
• Located near a major life sciences hub.
• Degree in Life Sciences, Computer Science, or related field.

Responsibilities

• Act as a trusted advisor to customers and clinical sites, ensuring trial designs meet goals and providing training and mentorship.
• Interpret clinical protocol requirements and project specifications, applying industry and Veeva best practices.
• Lead database development activities per the project plan, coordinating with sponsor, CRO, and other vendors.
• Coordinate with clinical data providers to configure data transfers.
• Configure forms, rules, and study items in Vault CDMS; build SQL-based listings for data cleaning.
• Run on-site or remote user acceptance testing, managing feedback and issue resolution.
• Support requirements gathering and specification writing for study integrations and go-live activities.
• Flag risks and contingency plans to project management to keep the project compliant.
• Contribute to process, product, and best-practice initiatives and support developers and testers.
• Share data management activities and feedback with the Vault CDMS product team.
• Configure and support data imports into Veeva DQS.

Skills

EDC software

SQL

Python

SAS

R

JSON

REST APIs

Life sciences domain

Client-facing

Project coordination

Veeva Vault CDMS

Data quality/data management

Education

Degree in Life Sciences, Computer Science, or related field

Tools

Vault CDMS

DQS

SQL

Job description

Veeva Systems is seeking a Senior Consultant with life sciences software programming experience to help customers maximize EDC on Vault CDMS. This full-time, remote-from-EU/UK role combines advisory and hands-on development, including data transfers, SQL listings, and UAT support.

You will work with sponsors, CROs, and data providers, applying Veeva best practices, and travel up to 10% as needed. A life sciences or CS degree is preferred with 5+ years in EDC and REST API experience.