Veeva Vault Clinical Consultant

Position: Veeva Vault Technical Lead Branchburg, NJ 6+ months Core responsibilities System Configuration: Set up and configure Veeva Vault applications, such as CDMS (for data management) or CTMS (for trial management). This includes configuring forms, edit checks, workflows, and roles. Clinical Processes: Apply a strong understanding of clinical trial processes, Good Clinical Practice (Google Cloud Platform), and regulatory requirements to configure the system to meet business needs. User Suppo

Job Title: Sr CQV/Validation Specialist Location:Raritan New Jersey 100% onsite Duration: 2+ Years Interview: 2 Virtual Interviews Job Description: We are seeking a Senior CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, riskbased validation aligned with USP <1058>, GAMP 5, and industry bes

Client needs candidates with active certifications only. It''s mandatory. Workday Time Management Consultant (Onsite Hybrid NJ)Expertise in Workday Time Tracking & Absence modulesExperience configuring time calculations, eligibility rules, and accrualsHands-on implementation/support experienceUnderstanding of payroll/time integration Client is not looking for visa candidates. Need independent candidates. Thanks Anju

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