This role is designed for a seasoned professional with deep expertise in the MedTech or Life Sciences space, specifically within clinical trial operations. You
Work type: remote
Location: Massachusetts - Boston
Salary: $80,000 – $200,000/yr
Type: Full-time
This role is designed for a seasoned professional with deep expertise in the MedTech or Life Sciences space, specifically within clinical trial operations. You should have at least 8 years of experience implementing complex software systems like CTMS or eTMF. The ideal candidate isn't just a technical expert but a strategic advisor who can lead global digital transformations for medical device and diagnostics companies. The position offers significant flexibility as a "Work Anywhere" role, allowing for full remote work provided you can travel up to 50% to client sites. The compensation range is exceptionally broad ($80k–$200k), reflecting the company's commitment to hiring for specific expertise. As a Public Benefit Corporation, the organization emphasizes a mission-driven culture that balances profit with social impact. **You might be a good fit if you:** * Have a proven track record of implementing clinical cloud solutions (e.g., Veeva Vault, Medidata, or Oracle Siebel). * Deeply understand the "day in the life" of clinical trial managers and the regulatory compliance requirements of MedTech. * Enjoy navigating complex stakeholder environments and translating business pain points into technical solution designs. * Are comfortable with a high-travel lifestyle to mentor project teams and lead customer engagements on-site.
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](https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6) (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
As a [Work Anywhere](https://careers.veeva.com/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](https://www.youtube.com/watch?v=TaPSP8cCSKY&ab_channel=Forbes), committed to making a positive impact on its customers, employees, and communities.
The Role
Veeva Systems is looking for consultants with system implementation experience and a passion for helping customers optimize their Clinical Operations data and document management processes.
Veeva’s Clinical Suite is the only unified suite of applications (eTMF, CTMS, Payments, Site Connect, Study Training) for clinical trial management from site selection to study archival, completely adapted for Medical Device, Research Organizations, and Diagnostics Companies of all sizes.
As a member of our Professional Services team, you will be responsible for understanding our customer’s current business processes and shaping future state vision, identifying and incorporating clinical needs, translating requirements into solution design, and defining global strategies to deploy our cloud-based solution across the enterprise.
Opportunities are available within the United States for this role, which is a remote position with a preference for Eastern or Central Time Zone. If a candidate is near an airport and able to meet travel requirements, there is no work location requirement. Qualified U.S.-based candidates are encouraged to apply.
## What You'll Do
Veeva Systems is looking for consultants with system implementation experience and a passion for helping customers optimize their Clinical Operations data and document management processes.
Veeva’s Clinical Suite is the only unified suite of applications (eTMF, CTMS, Payments, Site Connect, Study Training) for clinical trial management from site selection to study archival, completely adapted for Medical Device, Research Organizations, and Diagnostics Companies of all sizes.
As a member of our Professional Services team, you will be responsible for understanding our customer’s current business processes and shaping future state vision, identifying and incorporating clinical needs, translating requirements into solution design, and defining global strategies to deploy our cloud-based solution across the enterprise.
Opportunities are available within the United States for this role, which is a remote position with a preference for Eastern or Central Time Zone. If a candidate is near an airport and able to meet travel requirements, there is no work location requirement. Qualified U.S.-based candidates are encouraged to apply.