As a Veeva Vault Clinical - Validation Test Lead/Manager, you will be responsible for validating Veeva Vault Clinical systems with a focus on clinical trial processes and applications (eTMF, CTMS). You will drive test strategy, execution, manage testing efforts, validation documentation, and change control to ensure regulatory compliance and efficient delivery of clinical projects.
In this role, you will
• Develop validation and testing strategies tailored to system risk, complexity, and regulatory requirements, ensuring robust and compliant solutions.
• Estimate and plan testing efforts for projects and applications, evaluating requirements, defining test scope, and allocating resources appropriately.
• Oversee demand management by assessing project requests, prioritizing initiatives, and supporting efficient project planning and execution.
• Prioritize tasks based on business criticality, regulatory impact, and timelines to ensure effective delivery of clinical projects.
• Author and develop validation, testing, and qualification documentation—such as validation plans and reports, test plans and scripts, qualification plans, traceability matrices, and test error reports—ensuring all materials meet regulatory and quality standards.
• Review validation documentation to ensure accuracy, completeness, and compliance with internal and regulatory standards.
• Manage change control by assessing proposed changes, overseeing approvals, and tracking implementation. Coordinate assigned projects from initiation to closure, monitoring progress and resolving issues.
• Execute test procedures, document and analyze results, investigate test errors, and collaborate with relevant teams to resolve and retest as needed
Required skills
• Minimum 3–5 years of hands-on experience with Veeva Vault Clinical
• Experience in Computer System Validation (CSV), including developing validation protocols, performing risk assessments, executing validation testing, and ensuring compliance with GxP and regulatory standards.
• Demonstrated experience in the Life Sciences industry, with a strong understanding of industry standards, regulatory requirements, and best practices relevant to clinical operations and clinical applications.
• Solid understanding of the Clinical Operations domain, including study planning, conduct, and oversight processes.
• Strong understanding of Clinical Applications, such as electronic Trial Master File (eTMF), Clinical Trial Management Systems (CTMS), and other tools supporting clinical trial processes.
• Familiarity with regulatory submission processes, health authority correspondence, and the preparation of required documentation for clinical trial applications and approvals.
Preferred skills
Knowledge of AI assurance is an advantage, especially understanding how to validate and monitor AI-driven systems.
We're eager to meet people who share our mission and can make an impact in various ways. Don't hesitate to apply, even if you only meet the required skills listed. Your transferable skills and experiences matter—help us see how you the right person for this role.
Total compensation:
We regularly assess market data to ensure we offer a competitive compensation package for our associates. The base salary for this position ranges between CAD 90,000 – 110,000 per year. Where the successful candidate may fall within the range depends on relevant education, work and/or management experience and other business-related and job-necessary qualifications. This position is also eligible for Cognizant’s discretionary annual performance-based bonus, as well as benefits that support your physical, mental and financial wellbeing.
Working arrangements
We strive to provide flexibility wherever possible. Based on this role’s business requirements, this is a remote position open to qualified applicants in Ontario and/or Nova Scotia, where our hubs are located. Regardless of your working arrangement, we are here to support a healthy work-life balance though our various wellbeing programs.
The working arrangements for this role are accurate as of the date of posting. This may change based on the project you’re engaged in, as well as business and client requirements. Rest assured; we will always be clear about role expectations.
Cognizant will only consider applicants for this position who are legally authorized to work in Canada without requiring employer sponsorship, now or at any time in the future.
Applications for this position are reviewed by our recruitment team without the use of artificial intelligence screening tools.
私たちについて：
コグニザント（NASDAQ: CTSH）は、AI builderおよびテクノロジーサービスプロバイダとして、AI投資を企業価値へとつなげるフルスタックのAIソリューションを提供しています。業界、業務プロセス、エンジニアリングに関する深い専門性を強みに、各企業固有のコンテキストをテクノロジーシステムに組み込み、人の力を最大限に引き出すとともに、具体的な成果の創出と、急速に変化する世界におけるグローバル企業の競争力維持を支援します。詳しくは、当社ウェブサイト www.cognizant.com をご覧ください。
雇用に関する追加情報
本募集に記載されている報酬情報は、掲載日時点で正確なものです。Cognizantは、適用される法令に従い、いつでも本情報を変更する権利を留保します。
応募者は、対面またはビデオ会議による面接への参加を求められる場合があります。また、各面接の際に、現在有効な州政府または政府発行の身分証明書の提示を求められる場合があります。
Cognizantは機会均等雇用主です。応募および選考において、人種、肌の色、性別、宗教、信条、性的指向、性自認、国籍、障がい、遺伝情報、妊娠、退役軍人の地位、その他連邦法・州法・地方自治体の法律により保護されるいかなる特性に基づく差別も行いません。
