> Markdown version of [/jobs/ext/4634388-associate-director-of-it](https://www.wearedevelopers.com/jobs/ext/4634388-associate-director-of-it). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Associate Director of IT - **Company:** Intone Networks - **Location:** Redwood City, CA, United States - **Contract:** Permanent contract - **Skills:** Clinical Trial Management Systems, Data Migration, Enterprise Document Management System, IT Management, SAS (Software), System Testing, Systems Integration, Okta, Information Technology, Veeva, GXP, Servicenow - **Published:** November 8, 2026 - **Apply:** https://www.careerbuilder.com/job-details/associate-director-of-it-redwood-city-ca--f4742c1d-a3b2-4f64-aa8d-700f6c72c06a ## About the Role Computer Systems, System Validation, Team Lead/Manager, Biology, Project/Program Management, Multitasking, Environmental Sciences, Problem Solving Skills, Team Player, Validation Documentation, * Required * Previous experience leading a CSV program in a life sciences organization * Experience performing CSV activities such as defining validation scope, conducting risk assessments, developing URS, and managing validation documentation * Experience validating, using, and managing ongoing governance for Veeva QMS and QDS * Experience managing a Change Management platform project, preferably with ServiceNow, including driving process updates and platform qualification * Experience managing an SSO platform integration, preferably Okta * Experience developing data migration plans and executing or delegating migration protocols with understanding of compliance, traceability, and verification requirements * Experience with gap assessments, including owning remediation plan development and team delegation * Experience validating Veeva systems such as QDS, CRM, and RIMS * Preferred * SAS experience * Previous experience supporting audits and inspections with regulatory agencies * Experience reviewing CSV processes to ensure compliance with regulatory requirements and industry standards including GAMP 5, ITIL ISO, and ICH Technology Environment * Veeva: Quality Docs, RIM, eTMF, and QMS * CTMS and RTSM (Medidata preferred) * Okta SSO * ServiceNow * SAS ## Description This is a contract position for an Associate Director of IT based in Redwood City, California, with a duration of 6+ months. You will oversee Computer Systems Validation (CSV) initiatives while managing multiple concurrent projects in a life sciences environment, balancing strategic governance with hands-on delivery and team leadership. Responsibilities * Attend and participate in project maintenance, governance, status update, problem resolution, and timeline meetings * Manage 8-9 concurrent projects simultaneously * Perform direct contribution work, actively writing and delivering project deliverables * Review and approve team work, provide constructive feedback, and ensure problem resolution * Conduct bi-weekly one-on-one meetings with team members * Lead CSV program activities, including validation scope definition, risk assessments, User Requirements Specification (URS) development, and validation documentation management * Validate, implement, and manage ongoing governance for Veeva QMS and QDS systems * Lead Change Management platform projects, including process updates and platform qualification * Lead SSO platform integration initiatives * Develop data migration plans and execute or delegate migration protocols, ensuring compliance, traceability, and verification * Own gap assessments, develop remediation plans, and delegate execution to the team * Participate in IT leadership meetings and present project updates and risk assessments