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

Tired of working with old EDC technology? Looking for an opportunity to change how clinical trials, data and data are managed? Veevas Vault CDMS Electronic Data Capture (EDC) application will truly change how the industry runs clinical trials and we want you on our team!

As a Senior Technical Architect, you will be a leading member of the Veeva Systems Professional CDMS Services group working on providing consulting and technical architecture design on project teams implementing Veeva Vault CDMS (EDC) to companies in the life sciences industry.

As a key member of our Professional Services team, the Senior Technical Architect will lead customer implementations by providing expertise with Technical architecture design, technical integration design, and Vault CDMS (EDC) best practices. The Senior Technical Architect is a customer advocate working closely with other Veeva teams (Product, Sales, Strategy) to ensure customer success today and in the future.

This is a work anywhere, full-time permanent role with Veeva. Our work processes are designed so that you can be productive in the environment that works best for you. This is a customer-facing role and we have no work location requirement if you are in close proximity to an airport and able to meet future travel requirements.

Veeva Systems does not anticipate providing sponsorship for employment visa status (e.g., H-1B, OPT) for this employment position.

What You'll Do

Provide subject matter expertise on the Veeva Systems implementation, Vault CDMS (EDC) product suite, Vault Platform, technical design, and Software as a Service (SaaS) implementation best practices
Design and implement cloud-based integrations
Leading business process discovery and application design workshops
Taking complex client and Technical concepts and articulating them to audiences of varying perception levels
Design and provide subject matter expertise for development of custom applications
Manage integration and development projects and resources
Contribute to our professional services knowledge base
Develop internal and external tools to help our customers and our consultants
Partner with other parts of the organization to deliver technical presentations to current and prospective customers to evangelize the value of Veevas Technical
Support developers and testers during the project lifecycle
Support the requirements gathering and specification creation process for all study integrations
Support user acceptance testing with the customer for all custom integrations
Create user acceptance testing scripts (if applicable) for all custom integrations
Support go live activities for the study to ensure a smooth transition of the study to the customer
Review requirements as part of the change management process and update specifications and configurations as necessary with associated scoping activities
Act as the customers trusted advisor to ensure that the custom Technical is configured in such a way that it meets the customer's goals and offers the full benefits of Veevas CDMS (EDC) application
Notify project management of project risks and develop contingency plans as necessary
Ensure customer success from beginning to end of the project life cycle
Assure process compliance with all regulatory and Veeva procedural requirements
Participate and contribute to process, product, or best practices initiatives
Adherence to all Veeva and EDC Services procedures and policies

Requirements

5+ years direct experience working with EDC clinical software Technical in clinical operations, and/or trial management in a consultant role
5+ years direct experience with integrations such as IVRS/IRT, Coding Labs, Imaging, eCOA/Pro, etc.
2+ years experience in SAS/SDTM data extracts.
2+ years experience in writing custom reports.
Experience in interpreting clinical protocols and translating requirements into software specifications including writing and reviewing technical documentation
Experience in a customer-facing role, preferably with a software professional services organization or consulting background is preferred
Ability to quickly understand customer requirements and create corresponding Technical designs
Ability to articulate integration design patterns
Proven ability to manage diverse customers and/or stakeholders, and ensure delivery to a high degree of satisfaction
Working Knowledge of Clinical Trial processes across pharmaceuticals, device and/or biotech sectors, specifically as they relate to design, document, and data collection
Ability and willingness to roll up your sleeves to implement a clinical Technical
Ability to quickly understand business requirements
Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team
Logical approach to problem solving
Ability to manage multiple tasks and project deliverables
Proven track record of meeting project timelines/deliverables and attention to detail, process, deadlines, and quality results
Demonstrated success with customers during project assessment, planning, development, training and implementation.
Excellent verbal and written communication, interpersonal, and presentation skills
Expert on life sciences compliance and computer systems validation requirements
Ability to travel 25-30% (may include international)
4-year college degree required
Qualified candidates must be legally authorized to be employed in the United States. Veeva Systems does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

Nice to Have

Previous development experience with JAVA
Experience with document management platforms
Experience with GxP regulations and software validation process
Experience with source code control systems
Single Sign On experience
Life sciences industry experience and knowledge of clinical trial process preferred (pharmaceutical, biotech, medical device companies, CROs and academic & public health organizations).
Direct experience with EDC systems such as Medidata RAVE or Oracle/Phase Forward InForm
Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies
Life Science, computer science or related degree
Familiarity with CDISC, ODM and other data management industry standards
SaaS/Cloud experience in the delivery of clinical trials
Enterprise experience and knowledge transfer for running clinical trials with EDC
Consulting experience

Perks & Benefits

Flexible PTO
Allocations for continuous learning & development
Health & wellness programs

This is a remote position. This is a work anywhere, full time permanent role with Veeva. Our work processes are designed so that you can be productive in the environment that works best for you. This is a customer facing role and we have no work location requirement if you are in close proximity to an airport and able to meet future travel requirements.

#LI-Remote

#BI-Remote

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

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.