Veeva jobs

1.Certified would be required 2.Experience with configuration of Vaults

Veeva CTMS Location: Collegeville PA Duration: 9-12 Month JD: 1.Certified would be required 2.Experience with configuration of Vaults

TECHNOGEN, Inc. is a Proven Leader in providing full IT Services, Software Development and Solutions for 15 years. TECHNOGEN is a Small & Woman Owned Minority Business with GSA Advantage Certification. We have offices in VA; MD & Offshore development centers in India. We have successfully executed 100+ projects for clients ranging from small business and non-profits to Fortune 50 companies and federal, state and local agencies. Position: Veeva CRM Operations Analyst Location: Remote(Need from Ea

We are seeking experienced Product Owners and Business Analysts to support initiatives within the Life Sciences Cloud ecosystem, including Salesforce Health Cloud, Veeva, and related platforms. These roles will partner closely with product leadership, business stakeholders, and engineering teams to drive delivery across patient services, HCP engagement, and commercial capabilities. Candidates should bring strong domain understanding, adaptability across platforms, and the ability to quickly ramp

Job Title: Veeva CTMS Business Analyst Location: Foster City, CA (onsite) Duration: FTE (Immediate Need) Primary (must-haves): Business Analysis Leadership and Execution Lead complex, cross-functional initiatives related to Veeva Vault Clinical (CTMS/eTMF), including: implementation, optimization efforts, migrations, and strategic enhancements Convert ambiguity into clear problem statements, scope, success criteria, execution plans, timelines, risks, and decision points Proactively manage d

Veeva CRM Development EngineerLocation: Remote (must live in EST/CST time zones)Client Domain: Life SciencesDuration: 6 months, could extend to 12Interview Mode: videoJob Description:Senior hands-on contractor to design, build, and support commercial technology solutions across CRM, marketing, and patient/customer systems.8 years of CRM experience -must haveVeeva CRM/PromomatsDeliver end-to-end commercial system solutions (design through production)Configure and enhance CRM, marketing, and servi

NOTE: THIS IS NOT A CORP TO CORP JOB AND IT IS NOT A 1099 job; THIS JOB IS A W2 Salaried job- we cannot accommodate C2C or 1099. Thank you. Mindbank Job Opening Job Title: REDCap MetaData or Veeva Cloud Study Builder Work Permit Required: or for this government contract. Location: Bethesda, MD- 3 days on site and 2 days work from Home Hours: Monday - Friday - 40 hours per week Parking: Free at the building; great location and wonderful amenities Pay: 95,000 - 100,000.00 per year plus benefit

Must Have Technical/Functional SkillVeeva Vault Data Migration Experience: Hands-on End to End Veeva Data Migration experience on large data set (>500K records). Experience of using Vault Loader, Custom Migration Tool etc. Experience in data migration using Veeva API Expertise on Veeva Object Record Migration and Veeva Document Migration Expert knowledge of Veeva data model, including documents, records, and metadata. Experience on data map and transformation exercise from existing data sources

We are: The Advanced Technology Centers (ATCs) is the engine for reinvention in our clients' transformation journey. Powered by more than 255,000* people across 24 countries, ATCs will provide our clients seamless access to industry insights and innovative technology solutions. Stronger together! The Advanced Technology Centers (ATCs) make tremendous impact in solving our clients' business problems leveraging Innovation, Intelligence, Industry insights, new IT and new technology skills. Now,

Job Description About the Role We are seeking a Software Engineer with hands-on experience in Veeva Vault Clinical to design, build, and support integrations, data pipelines, and reporting across the Clinical Suite. The ideal candidate has practical expertise with Vault Loader, Veeva APIs, Postman, MuleSoft integrations, and connectors, along with working knowledge of the Vault Clinical object model. You will partner with Clinical Operations, Quality, and IT to deliver secure, scalable solutio

It's More Than a Career, It's a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives

Key Responsibilities For Product Owners Own and manage the product backlog, aligning with business priorities and roadmap. Translate business objectives into epics, features, and user stories with clear acceptance criteria. Act as the primary liaison between stakeholders and delivery teams. Drive sprint planning, backlog grooming, demos, and retrospectives. Ensure alignment across business, product, and engineering teams. Support delivery across Life Sciences Cloud platforms and associated ecosy

Summary: Our client is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate must have hands-on experience with Veeva platforms and data migration projects in regulated pharma environments. Roles & Responsibilities: Validating Veeva platforms within a pharmaceutical company Developing UAT documents and writing test scripts Managing change controls including creation, e

Job Summary: Experienced CSV (Computer System Validation) Consultant with expertise in GxP-compliant environments to support validation, compliance, and audit readiness across life sciences systems. Strong experience in CSV processes, regulatory frameworks, validation documentation, and exposure to clinical and regulatory domains.Roles & Responsibilities: Perform Computer System Validation (CSV) activities aligned with 21 CFR Part 11 / 820, GxP, GAMP 5, SOX, EU Annex 11 / Annex 22, ISO 9001, an

Swing shift - candidates need to have flexibility for different shifts. Dayshift / Nightshift / Weekend 10% travel required - Must be able to travel internationally for work (Europe/Canada) 18 month contract to start Ideal Candidate: B.S. and 4 years of GMP experience, Packaging equipment experience, technical writing & Document management system experience - KNEAT or Veeva highly preferred The Senior Process Development Engineer - Packaging Equipment supports commercial GMP Final Drug Produc

Description We are looking for a Digital Project Manager to lead a diverse portfolio of digital initiatives for pharmaceutical and medical education clients in New Jersey. This Long-term Contract position offers the opportunity to oversee mobile, multimedia, content-driven, and event-related interactive projects while partnering with cross-functional teams to keep work on track. The ideal candidate brings strong project leadership, comfort working in regulated industries, and the ability to mana

Summary : We are seeking an experienced Validation Engineer to support pharmaceutical manufacturing and quality operations in Washington. The ideal candidate will have hands-on experience in equipment, process, cleaning, and computerized system validation within a GMP-regulated pharmaceutical environment. This role requires strong knowledge of validation lifecycle activities, regulatory compliance, documentation, and cross-functional collaboration. Roles & Responsibilities : Execute and support

Job Location MASON BUS AND INNOVATION CTR Job Description Research and Development (R&D) at Procter & Gamble, the largest consumer packaged goods company in the world, includes a diverse group of roles that contribute to the innovation and development of our products. It encompasses roles in product research, formulation, testing, and scientific analysis. You will find variety and excitement starting Day 1. The Opportunity: P&G has an opportunity for a Laboratory Animal Scientist to join our Gl

Job Summary: The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys Client. By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring

Job Summary: The CSV Engineer / Validation Engineer will be responsible for ensuring computerized systems in a regulated pharmaceutical environment comply with GxP, 21 CFR Part 11, GAMP 5, EU Annex 11, ISO 9001, and SOX requirements. The role involves supporting validation activities using a risk-based approach aligned with CSA principles, ensuring systems are audit-ready, and maintaining compliance throughout the system lifecycle. The position also requires hands-on involvement in documentatio