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Senior Consultant - Clinical Data Programming

Remote, Barcelona·Full-time·Added 23 days ago

Veeva

66 open roles

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Overview

Job details

  • €72,000 - €110,000 a year

    Gross, as stated in the ad.

    About €4,050 - €5,790 a month after tax, or €4,240 - €6,650 under the Beckham regime.

  • Full-time hours

    Per the ad.

  • Fully remote

    Only from certain places, per the ad: “open to candidates working remotely from the EU or UK”

Requirements

  • Have the right to work in Spain

    Veeva doesn't mention sponsorship in the ad.

  • Work in English

    English is required, per the ad.

  • Have 5+ years of experience

    Mid-level role.

The role

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.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

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

What we're looking for

  • 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

Pay & benefits

What you'll get

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

Visa & relocation

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.

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.

Hiring process

4 steps3 interviewsa task to do

  1. Submit your resume

  2. Personality assessment

    With a third party · Online test

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

  3. Application review · With our team

  4. A conversation with the hiring manager

    With a hiring manager

  5. A practical case exercise

  6. A final conversation with our group's Senior Leader

    With a group's Senior Leader

  7. Final decision · With a hiring manager

  • Some adverts instead list the personality assessment as a step inside the interview stage, without the three-day promise.
  • We value your time and believe in a transparent hiring process.

Hiring process

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.

About Veeva

Veeva Systems is a leading cloud-computing company focused on the life sciences and pharmaceutical industries, providing software solutions for clinical, regulatory, quality, and commercial operations. Founded in 2007 and headquartered in Pleasanton, California, Veeva has grown into a global technology leader with over 6,000 employees, serving more than 1,000 customers worldwide, including most of the top pharmaceutical companies. Its products, such as Vault, CRM, and OpenData, are industry standards for managing content, data, and customer relationships in the life sciences sector.

In Spain, Veeva has a significant presence, with offices in Barcelona and Madrid, and is actively hiring for a wide range of roles, from entry-level consultants to senior directors. The company is known for its strong culture of innovation, employee development, and work-life balance, offering remote and hybrid work options. For international professionals, Veeva provides an opportunity to work with cutting-edge technology in a dynamic, global environment, with a strong emphasis on career growth and learning. The Spanish offices are key hubs for its European operations, particularly in consulting, data operations, and marketing, making it an attractive destination for talent from around the world.

Industry
HealthTech
Founded
2007
Employees
5,000–10,000
Headquarters
Pleasanton, USA
In Spain
Barcelona, Madrid
Website
veeva.com

Good to know if you are moving

  • Veeva has offices in Barcelona and Madrid, with Barcelona being the main hub for its European operations, offering a vibrant city life and a growing tech scene.
  • The company offers remote work options for many roles, providing flexibility for international hires.
  • Veeva is known for its strong company culture, with a focus on employee development, and has been recognized as a great place to work in multiple countries.
  • The company provides a structured onboarding and training program for new consultants, including a 'Master Class' series for entry-level positions.
  • Veeva's global presence and industry leadership offer opportunities for career advancement and international mobility.

In their own words

About the company & team

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 [email protected].

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