ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. 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.
Our most valuable asset is our people.
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 part of your success here. Learn more about our diversity, equity, and inclusion efforts and the networks ZS supports to assist our ZSers in cultivating community spaces, obtaining the resources they need to thrive, and sharing the messages they are passionate about.
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