3 Vault Loader Jobs

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage and passion to drive life-changing impact to ZS. ZS Life Science R&D Technologist in Clinical development ZS life science R&D team partners with clients to discover and develop innovative medicines that improve patient's lives. Our work spans consulting, analytics and technology (services and platforms) projects across the several domains. We have 3500+ zs professionals that deliver R&D programs, $100MM+ invested in R&D data, analytics and technology assets and 100+ clients on R&D programs. Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in drug development. The Drug Development R&D Technologists possess a deep understanding of technological solutions for clinical development processes including clinical study design, data management, analytics, and quality risk management platforms and products. They are well-versed in software related to clinical trial protocol design, electronic data capture (EDC), external data capture, data conformance, transformation, analysis, and reporting. Our team is well versed about industry standards such as CDISC, FHIR, OMOP, and their respective usage. Our team specializes in designing bespoke solutions or products implementation for clinical design, data management, and analytics systems. Our team has deep understanding of EDC tools like Rave, Veeva, InForm, openClinica, clinical data repositories like SAS LSAF, Oracle LSH, eCS elluminate, Metadata Repositories like Nurocor, Sycamore, Formedix, statistical computing environments like Sycamore, Domino, Sas Viya systems, Clinical data review systems, RBQM systems, and more. With experience as solution architects, business analysts, or techno-functional SMEs in GXP compliant validated environments, they guide the creation of solution, data flows and strategies for building clinical development and data management systems. Their offerings encompass technical advisory, consultancy, developing of clinical data platforms and products, system integration, and intelligent automation. Additionally, the team has created innovative tools through advanced technology and data science, aiding numerous clients in expediting the drug development process. We are seeking a highly experienced Technical Architect with deep expertise in Veeva Vault R&D solutions to join our team. The ideal candidate will have a strong background in clinical and operational R&D systems and datasets, with a proven track record in delivering end-to-end Veeva Vault migration and integration projects. This individual will lead technical engagements, architect solutions, and provide hands-on support for data migration, system integration, and customization initiatives in regulated life sciences environments. Key Responsibilities: Serve as the technical lead on Veeva Vault R&D implementations, upgrades, and migration projects. Architect and lead data migration strategies for Development Vaults, including cutover planning and phased deployment designs. Design and implement integrations to and from Vault R&D products (e.g., Vault Clinical to data lakes or other systems). Conduct data quality assessment, cleansing, STTM transformation, ingestion, and validation for clinical and operational datasets. Develop and maintain custom Vault API scripts and implement Vault Loader methodologies for automated data operations. Collaborate with cross-functional stakeholders including clinical, regulatory, and IT teams to ensure compliance and alignment with business needs. Execute system validation and testing procedures in accordance with GxP and CFR Part 11 guidelines. Proficient in Vault Loader, Vault API scripting, and hands-on Vault configuration/customization. Solid understanding of clinical trial data, operational workflows, and life sciences regulatory environments. Strong problem-solving skills with the ability to architect scalable, compliant, and sustainable solutions. Required Qualifications: 8+ years of experience with Veeva Vault R&D products, including Vault Clinical. Demonstrated expertise in leading data migration and integration projects as a Technical Architect or similar role Perks & Benefits: ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth and professional development. Our robust skills development programs, multiple career progression options and internal mobility paths and collaborative culture empowers you to thrive as an individual and global team member. We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections. Travel: Travel is a requirement at ZS for client facing ZSers business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures. Considering applying At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems-the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are integral to your success here. We are committed to building a team that reflects a broad variety of backgrounds, perspectives, and experiences. about our inclusion and belonging efforts and the networks ZS supports to assist our ZSers in cultivating community spaces and obtaining the resources they need to thrive. If you're eager to grow, contribute, and bring your unique self to our work, we encourage you to apply. ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law. To complete your application: Candidates must possess or be able to obtain work authorization for their intended country of employment.An on-line application, including a full set of transcripts (official or unofficial), is required to be considered. NO AGENCY CALLS, PLEASE. Find Out More At:

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage and passion to drive life-changing impact to ZS. ZS Life Science R&D Technologist in Clinical development ZS life science R&D team partners with clients to discover and develop innovative medicines that improve patient's lives. Our work spans consulting, analytics and technology (services and platforms) projects across the several domains. We have 3500+ zs professionals that deliver R&D programs, $100MM+ invested in R&D data, analytics and technology assets and 100+ clients on R&D programs. Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in drug development. The Drug Development R&D Technologists possess a deep understanding of technological solutions for clinical development processes including clinical study design, data management, analytics, and quality risk management platforms and products. They are well-versed in software related to clinical trial protocol design, electronic data capture (EDC), external data capture, data conformance, transformation, analysis, and reporting. Our team is well versed about industry standards such as CDISC, FHIR, OMOP, and their respective usage. Our team specializes in designing bespoke solutions or products implementation for clinical design, data management, and analytics systems. Our team has deep understanding of EDC tools like Rave, Veeva, InForm, openClinica, clinical data repositories like SAS LSAF, Oracle LSH, eCS elluminate, Metadata Repositories like Nurocor, Sycamore, Formedix, statistical computing environments like Sycamore, Domino, Sas Viya systems, Clinical data review systems, RBQM systems, and more. With experience as solution architects, business analysts, or techno-functional SMEs in GXP compliant validated environments, they guide the creation of solution, data flows and strategies for building clinical development and data management systems. Their offerings encompass technical advisory, consultancy, developing of clinical data platforms and products, system integration, and intelligent automation. Additionally, the team has created innovative tools through advanced technology and data science, aiding numerous clients in expediting the drug development process. We are seeking a highly experienced Technical Architect with deep expertise in Veeva Vault R&D solutions to join our team. The ideal candidate will have a strong background in clinical and operational R&D systems and datasets, with a proven track record in delivering end-to-end Veeva Vault migration and integration projects. This individual will lead technical engagements, architect solutions, and provide hands-on support for data migration, system integration, and customization initiatives in regulated life sciences environments. Key Responsibilities: Serve as the technical lead on Veeva Vault R&D implementations, upgrades, and migration projects. Architect and lead data migration strategies for Development Vaults, including cutover planning and phased deployment designs. Design and implement integrations to and from Vault R&D products (e.g., Vault Clinical to data lakes or other systems). Conduct data quality assessment, cleansing, STTM transformation, ingestion, and validation for clinical and operational datasets. Develop and maintain custom Vault API scripts and implement Vault Loader methodologies for automated data operations. Collaborate with cross-functional stakeholders including clinical, regulatory, and IT teams to ensure compliance and alignment with business needs. Execute system validation and testing procedures in accordance with GxP and CFR Part 11 guidelines. Proficient in Vault Loader, Vault API scripting, and hands-on Vault configuration/customization. Solid understanding of clinical trial data, operational workflows, and life sciences regulatory environments. Strong problem-solving skills with the ability to architect scalable, compliant, and sustainable solutions. Required Qualifications: 8+ years of experience with Veeva Vault R&D products, including Vault Clinical. Demonstrated expertise in leading data migration and integration projects as a Technical Architect or similar role Perks & Benefits: ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth and professional development. Our robust skills development programs, multiple career progression options and internal mobility paths and collaborative culture empowers you to thrive as an individual and global team member. We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections. Travel: Travel is a requirement at ZS for client facing ZSers business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures. Considering applying At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems-the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are integral to your success here. We are committed to building a team that reflects a broad variety of backgrounds, perspectives, and experiences. about our inclusion and belonging efforts and the networks ZS supports to assist our ZSers in cultivating community spaces and obtaining the resources they need to thrive. If you're eager to grow, contribute, and bring your unique self to our work, we encourage you to apply. ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law. To complete your application: Candidates must possess or be able to obtain work authorization for their intended country of employment.An on-line application, including a full set of transcripts (official or unofficial), is required to be considered. NO AGENCY CALLS, PLEASE. Find Out More At:

Primary Skills (Must have expereince): 6+ years of experience in Veeva Vault platform, with at least 23 years in Veeva Vault RIMS support and configuration. 4+ years of experience in Veeva Vault RIMS modules including Registrations, Submissions, Correspondence, and Commitments. 4+ years of hands-on experience in managing L2/L3 support activities including ticket triaging, incident/problem/change management. 4+ years of experience in Vault configuration: document types, object configuration, workflows, lifecycles, security policies. 4+ years of experience in managing system performance, error handling, and integration troubleshooting. 3+ years of experience with Veeva Vault admin console, security roles, and permission sets. 3+ years of experience in Veeva support tools (MyVeeva, Vault Loader, VQL, Vault REST APIs). 3+ years of experience in leading a support team and working in a multi-vendor global delivery model. Role & responsibilities As the Team Lead, you will be responsible for managing the end-to-end application maintenance lifecycle for Veeva Vault RIMS, including incident management, problem resolution, change requests, enhancements, release management, system configuration, and user support. You will coordinate with client stakeholders, Veeva product teams, and cross-functional IT teams to resolve issues and implement solutions that align with business objectives and compliance standards. You will lead a team of support engineers and administrators who handle daily operational activities such as resolving tickets, addressing integration issues, monitoring system health, managing access controls, and troubleshooting performance-related concerns. You are expected to define SLAs and ensure adherence, analyze recurring issues, recommend preventive actions, and continuously improve the support framework using ITIL best practices. Your leadership will be critical in planning and executing minor enhancements and releases, conducting impact assessments for upgrades, regression testing, and preparing business readiness documentation. You will serve as the escalation point for complex technical or functional issues, working in close collaboration with business analysts, quality assurance, and regulatory affairs teams. Additionally, you will assist in training and onboarding support team members, mentoring them on Veeva Vault RIMS functionality, configuration options, and standard operating procedures. You will also participate in governance meetings and provide regular reporting on performance metrics, open risks, resource utilization, and improvement opportunities. A deep understanding of regulatory submission management, registration tracking, health authority correspondence, and product lifecycle management processes is essential. Your technical expertise should span Veeva Vault RIMS modules, Vault configuration tools, document types, security policies, workflows, lifecycle states, and reporting tools. The role also demands excellent stakeholder management, communication, and documentation skills. You should be proactive, solution-oriented, and have a track record of delivering results in a global delivery model with cross-functional teams.