Senior Clinical Consultant

hace 6 días

Barcelona, España Veeva Systems A tiempo completo

Veeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster. We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed. Our teams develop transformative cloud software, services, consulting, and data to make our customers more efficient and effective in everything they do. Veeva is a work anywhere company. You can work at home, at a customer site, or in an office on any given day. As a
**Public Benefit Corporation**, you will also work for a company focused on making a positive impact on its customers, employees, and communities.

**The Role**

Do you love solving business problems with technology? Are you passionate about enabling Clinical Operations to conduct studies faster and more efficiently? Come help us transform Clinical Trials management in the MedTech industry

**What You’ll Do**
- Lead implementation projects of the Vault Clinical suite for MedTech companies (including Vault eTMF, Vault CTMS, and Vault Payments).
- Conduct requirements workshops, design, and configuration review iterations with our customers’ Clinical Operations and IT stakeholders. Ensure adherence to the industry best practices.
- Look after customers’ success from the beginning to the end of the engagement.
- Mentor project team members and junior consultants.
- Provide insight and recommendations to improve our technology and solutions for the MedTech industry by working closely with our Product team.

**Requirements**:

- 8+ years of relevant work experience in the Life Science (MedTech, Pharma, Biotech) or Healthcare industry
- Deep knowledge of Clinical Study management, regulatory and operations processes, data, and documentation requirements.
- Self-starter and motivated individual with the proven ability to work independently in a dynamic environment.
- Proven ability to manage diverse customers and/or stakeholders, ability to communicate to all levels of an organization, and to ensure project delivery to a high degree of satisfaction and quality.
- 4-year degree or equivalent work experience required.
- Ability to travel up to 40%.

**Nice to Have**
- Computer Science, Life Science or related degree preferred.
- Work experience in the Medical Device or Diagnostics space
- Familiarity with MedTech Quality Systems regulatory requirements and guidelines: ISO 13485, 2017/745, 2017/746, 21 CFR Part 11, GAMP
- Direct experience with regulated document
- Experience in Services Delivery Management and Pre-Sales presentations with SaaS/Cloud
- PMP/Agile certification

**Perks & Benefits**
- Allocations for continuous learning & development
- Health & wellness programs

RemoteSpain

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

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.

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