Senior Consultant - Clinical Data Programming

Veeva's Vault Clinical Data Management System (CDMS) is changing how life sciences companies manage clinical trial data, bringing EDC, coding, and Veeva Data Quality System (DQS) together in one platform. We're looking for a Senior Consultant with life sciences software programming experience to help customers get the most out of EDC while running their trials. This is a full-time, permanent, customer-facing role open to candidates working remotely from the EU or UK.

Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship along the way

Work with customers to 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 vendor teams

Coordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data transfers

Configure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings for customer data cleaning needs

Run on-site or remote user acceptance testing, managing feedback, issue resolution, and study acceptance

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 with regulatory and Veeva procedures

Contribute to process, product, and best-practice initiatives, and support developers and testers throughout the project lifecycle

Share data management activities, challenges, and end-user feedback with the Vault CDMS product team

Configure and support data imports into Veeva DQS

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 languages such as SAS, R, JSON, Python, or SQL, with the ability to pick up new SQL-based languages

Background in the life sciences industry (pharma, biotech, medical device, CRO, or academic/public health), with experience across project assessment, planning, development, training, and implementation

Experience in a customer-facing role, ideally within software professional services or consulting

Ability to work independently and collaboratively in a 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

Familiarity with data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM)

Experience working 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, including technical documentation

Experience with Veeva applications

Located near a major life sciences hub

Degree in Life Sciences, Computer Science, or a related field

We value your time and believe in a transparent hiring process. Here is the process you can expect.

Follow the application process and submit your resume.

Within 3 days, you will receive a link to a personality assessment administered by a third party.

Once you complete the assessment, our team will review your full application package and follow up via email with our decision.

If moving to the interview stage, the process is as follows:

1. A conversation with the hiring manager
2. A practical case exercise
3. A final conversation with our group's Senior Leader.

Once all interviews are complete, the manager will be in touch with a final decision.

Private health insurance

Flexible paid time off plus local public holidays

Pension / retirement plan contributions

1% charitable giving program