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Senior Consultant - Clinical Data Programming

Veeva Systems veeva.com Open · verified Oct 24, 2026
Remote Barcelona Full-time Senior Other

At a glance

Senior role at Veeva Systems. Remote, Spain · full-time · €72,000–€110,000 OTE.

On-target earningsStated by Veeva Systems
€72,000 – €110,000
On-target earnings for this role, in EUR per year, as published in the posting. Base plus commission; the split is in the posting.
RoleOther
SenioritySenior
LocationBarcelona
WorkplaceRemote
EmploymentFull-time
OTE€72,000–€110,000
PostedSep 1, 2026 · 7w ago
Role brief

remoteroles summary, based on the employer's posting.

What you'll do

  • Guide customers and clinical sites through study setup, helping configure trial designs and building their skills with training
  • Turn clinical protocols and project specifications into database plans, then coordinate development with sponsors, CROs and vendors
  • Set up Vault CDMS forms, rules and study elements, and create SQL listings that help customers clean trial data
  • Coordinate data transfers from clinical providers and run acceptance testing, resolving feedback and issues through study approval
  • Write integration requirements, support go-live and data imports into Veeva DQS, and raise project risks with contingency plans

What you bring

  • At least five years using EDC clinical software across database design, collection, analysis, query resolution, datasets and statistical reporting
  • Programming ability in SQL, SAS, R, JSON or Python, plus readiness to learn new SQL-based languages
  • You understand clinical trial data collection and review, and have worked in life sciences across project delivery
  • You have customer-facing experience and can communicate clearly while meeting project timelines

Who this fits

This senior, customer-facing consulting role suits someone who can work independently and with project teams across the full study lifecycle. It is remote for candidates based in the EU or UK, with travel of up to ten percent that may be international.

From the employer

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment. Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

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.

What You’ll Do

  • 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

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 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

Nice to Have

  • 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

Interviewing with Veeva

    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.

Perks & Benefits

  • Private health insurance
  • Flexible paid time off plus local public holidays
  • Pension / retirement plan contributions
  • 1% charitable giving program

Compensation

  • Total compensation: 72,000 - 110,000 EUR
  • The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus.
#RemoteSpain
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com.
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Opportunity

Other work from LinkedIn, X, Reddit and Upwork, in one list.

Each morning you get everything that fits, strongest first.

Find me work

By the team behind remoteroles.