4 часа назад
Senior IT Analyst II - IT Research and Development (Veeva Vault)
157 800 - 195 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior IT Analyst II - IT Research and Development (Veeva Vault): Leading regulatory IT systems for Global Regulatory Affairs, with an accent on Veeva Vault RIM administration, system ownership, integrations, compliance, and production support. Focus on translating business and technical requirements, managing system lifecycles and vendor implementations, and delivering validated solutions in a regulated pharmaceutical environment.
Location: United States — Remote. The role is officially full-time from home, with occasional travel to offices or other locations as needed.
Annual salary: $157,800–$195,000 USD, plus eligibility for annual bonus and equity incentives.
Company
is a biopharmaceutical company developing innovative treatments for rare diseases and supporting patients through a collaborative, science-driven model.
What you will do
- Own regulatory IT systems and serve as the primary IT contact for Global Regulatory Affairs.
- Maintain IT roadmaps, assess business demand, and align regulatory technology initiatives with business priorities.
- Lead system maintenance, enhancements, release planning, implementations, and vendor issue resolution.
- Manage production support, incident and problem management, service management, and performance monitoring.
- Deliver technical integrations by defining data mappings, integration requirements, validation rules, and publishing or subscription models.
- Coordinate vendor selection, third-party risk assessments, IT compliance, budgets, and GxP-aligned delivery.
Requirements
- Bachelor’s degree in Information Technology, Computer Systems, Information Systems, or a related field.
- 7+ years of relevant experience with Regulatory IT R&D systems.
- Hands-on experience with the Veeva Vault RIM suite, including Vault Registrations, Vault Submissions, Vault Submissions Archive, and Vault Publishing.
- Experience providing technical solutions, reviewing vendor designs, working with SDLC in regulated environments, and testing applications against requirements.
- Knowledge of regulatory processes such as submission planning and tracking, registration management, commitment management, and content management.
- Experience leading cross-functional teams and working with vendors or managed service providers in a matrix environment; pharmaceutical experience and knowledge of GxP, xEVMPD, IDMP, and SPOR are valuable.
Nice to have
- Veeva-certified Vault owner training and experience managing non-Veeva applications.
- Experience with Lorenz Docubridge, Lorenz eValidator, eCTD submission systems, CDER Direct, ESG Webtrader, eSubmission Gateway, Eudralink, IRIS, or similar regulatory systems.
- Pharmaceutical industry experience and knowledge of data standardization requirements.
Culture & Benefits
- Remote work from home with occasional business travel.
- Vacation time and company-observed public holidays.
- Volunteer days, wellbeing benefits, and fitness reimbursement.
- Long-term incentive and employee stock purchase plans or equivalent offerings.
- Tuition sponsorship and professional development plans.
- Benefits vary by region and country.
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