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 $2B 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 RoleWe 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 membersClosely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear testable and compliant formatEnsure requirements are adequately tested following a risk-based approachDevelop and maintain CSV deliverables including requirements specifications test scripts summary reports and trace matricesManage Validation testing cycles and resolution of issues and enhancement requestsMaintain change control documentation to ensure ongoing validation of the RTSM systemProvide technical expertise to RTSM team members in computer system validation applicable regulations and other quality system requirementsSupport 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 11Exceptional attention to detailGood interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levelsExperience with authoring automation testing using Selenium Nice to Have ➡ Familiarity with the conduct of clinical trialsPrevious experience with RTSMExpert in Microsoft Word and Excel Perks & Benefits ➡ Medical dental vision and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving program Compensation ➡ Base pay: $60000 - $100000The 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-RemoteVeeva’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.

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 $2B 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 RoleWe 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 membersClosely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear testable and compliant formatEnsure requirements are adequately tested following a risk-based approachDevelop and maintain CSV deliverables including requirements specifications test scripts summary reports and trace matricesManage Validation testing cycles and resolution of issues and enhancement requestsMaintain change control documentation to ensure ongoing validation of the RTSM systemProvide technical expertise to RTSM team members in computer system validation applicable regulations and other quality system requirementsSupport 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 11Exceptional attention to detailGood interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levelsExperience with authoring automation testing using Selenium Nice to Have ➡ Familiarity with the conduct of clinical trialsPrevious experience with RTSMExpert in Microsoft Word and Excel Perks & Benefits ➡ Medical dental vision and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving program Compensation ➡ Base pay: $60000 - $100000 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-RemoteVeeva’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.