Job description

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 We are looking for a Computer Software Validation (CSV) professional with a specialty in clinical trial software. This role would give you the opportunity to work on a leading solution in Randomization and Trial Supply Management (RTSM) software and help our customers bring treatments to patients faster. To excel in this role you will require strong technical writing capabilities and the ability to simplify complex topics. As a member of the RTSM team, you will work closely with Development and Project Management teams to support customer RTSM implementations in a fast-paced environment. You will use your expertise to take ownership of the validation process for assigned projects and play an important role in building and maintaining product excellence for the RTSM system. This is a remote role with Veeva's Work Anywhere policy allowing you to 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. What You'll Do Participate in RTSM requirement gathering sessions with clients and RTSM team members Closely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant format Ensure requirements are adequately tested following a risk-based approach Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices Manage Validation testing cycles and resolution of issues and enhancement requests Maintain change control documentation to ensure ongoing validation of the RTSM system Provide technical expertise to RTSM team members in computer system validation, applicable regulations, and other quality system requirements Support customers as needed in RTSM validation activities Requirements 1+ year of experience in a CSV for clinical trial software (CTMS, CDMS, eTMF, etc.) Working knowledge of software development cycle (SDLC) Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11 Exceptional attention to detail Good interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levels Nice to Have Familiarity with the conduct of clinical trials Previous experience with RTSM Expert in Microsoft Word and Excel 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 manager A practical case exercise A 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 Medical, dental, vision, and basic life insurance Flexible PTO and company paid holidays Retirement programs 1% charitable giving program Compensation Base pay: $ 60,000 - $100,000 The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries 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 may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus. #LI-Remote #LI-Associate Veeva’s 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. 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 talent_accommodations@veeva.com .

Requirements

Must-haves

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.
This is a remote role with Veeva's Work Anywhere policy allowing you to 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.
Participate in RTSM requirement gathering sessions with clients and RTSM team members
Closely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant format
Ensure requirements are adequately tested following a risk-based approach
Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices
Manage Validation testing cycles and resolution of issues and enhancement requests
Maintain change control documentation to ensure ongoing validation of the RTSM system
Provide technical expertise to RTSM team members in computer system validation, applicable regulations, and other quality system requirements
Support customers as needed in RTSM validation activities
1+ year of experience in a CSV for clinical trial software (CTMS, CDMS, eTMF, etc.)

Nice-to-haves

Familiarity with the conduct of clinical trials
Previous experience with RTSM
Expert in Microsoft Word and Excel
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 manager
A practical case exercise
A final conversation with our group's Senior Leader.

Application prep

Use the role’s language and application details while tailoring your materials.

Keywords to mirror

gcp

Platform: lever
Effort: quick

Benefits

Benefits detected in the listing.

Dental

Vision

Pto