Team: Professional Services

Country:
Spain Remote Work Available: Yes
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 DoAct 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 DQSRequirements5+ 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 APIsExperience 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:
A conversation with the hiring managerA practical case exerciseA 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

Adaptable paid time off plus local public holidays

Pension / retirement plan contributions1% charitable giving program

Compensation

Total compensation:



72,000 - 110,000 EURThe 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.#Remote

Spain#LI-Mid

Senior

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 Where It’s Best for You

Work Anywhere means you can work in an office or at home on any given day.

It’s about getting the work done in the way and place that works best for each person.

This applies across all locations and departments.

Work Anywhere does not mean work at any time.

We have predictable core hours where employees are generally available for meetings and collaboration.

Employees are focused and available during core hours.

We invest in our offices to make them places where our employees like to go.

If you work in the office three or more days a week, you will have a dedicated office workspace.

Our offices function as hubs to draw people in, create social bonds, and where random connections and mixing of ideas happen.

We’re investing more in offices, culture, and offsite meetings, not less.

Product teams are organized in regional product hubs for optimal collaboration and live within a time zone of their hub.

Our current product hubs are located in Pleasanton, Columbus, Boston, Kansas City, New York City, Raleigh, and Toronto.

We create opportunities for teams to get together in person regularly.

Customer-facing roles, such as Sales and Professional Services, live near and/or travel to their customers.

When an employee moves within a country it does not cause a change in salary.

Where you live impacts you and your family.

Not knowing if your compensation will change if you move can cause stress and uncertainty for everyone.

We wanted to eliminate that.

Work at Veeva.

Work where it’s best for you.

📌 Senior Consultant - Clinical Data Programming (España)
🏢 Veeva Systems
📍 España