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Чётко очерченная ведущая роль в крупной биотех-компании даёт возможность работать с клиническими системами, но узкая специализация на Veeva может ограничить выбор следующих карьерных шагов.
?Узкая специализация
Понятные задачи
Крупная компания
Клинические технологии
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Clinical Systems Business Analyst (Veeva ClinOps): Supporting the Veeva ClinOps suite for clinical trial management by defining business requirements, processes, data needs, and test plans with an accent on regulatory alignment, product backlogs, and software delivery. Focus on analyzing Veeva upgrades, writing user stories and acceptance criteria, validating implementations, and collaborating with architects, product managers, developers, vendors, and business stakeholders.
Location: Portugal - Lisbon; Flex Commuter / Hybrid
Salary: €50,417.75–€68,212.25
Company
hirify.global is a global healthcare organization with a Lisbon capability center supporting areas including clinical technology, cybersecurity, data and analytics, digital, and innovation.
What you will do
Support the Clinical Trial Management, Monitoring, and Engagement product team as a technical subject-matter expert for the Veeva ClinOps suite.
Gather, refine, and document business and non-functional requirements, user stories, business process maps, technical and functional requirements, and test plans.
Capture customer needs, define business processes and product requirements, and maintain accurate configuration, process, and change documentation.
Analyze Veeva version upgrades, assess their impact, refine product and release backlogs, and ensure requirements are prioritized.
Partner with architects, Product Managers, Technical Product Owners, developers, vendors, business partners, and hirify.global IT teams to plan and deliver software solutions.
Develop business cases for digital innovation opportunities, execute product demonstrations, and provide feedback to ensure delivered software meets requirements.
Requirements
Doctorate degree, or a master’s degree with 4–6 years of experience, bachelor’s degree with 6–8 years of experience, or diploma with 10–12 years of experience in Computer Science, IT, or a related field.
Experience with the Veeva ClinOps suite of applications.
Experience with the SAFe Framework and Agile software development methodologies.
Experience writing requirements for modern web applications, including user requirements and acceptance criteria in agile project management systems such as JIRA.
Excellent problem-solving skills and the ability to tackle complex challenges in drug discovery with technology.
Excellent communication skills, including the ability to interface with senior leadership with confidence and clarity.
Ability to work under minimal supervision, manage multiple priorities, and collaborate effectively with global virtual teams.
Strong analytical, gap and fit assessment, verbal and written communication, presentation, and public speaking skills.
Ability to provide oversight and mentoring, delegate work, show initiative and self-motivation, and contribute to team goals.
Nice to have
Expertise in a scientific domain and related technology needs, or understanding of scientific software systems strategy, governance, and infrastructure.
Experience with the Veeva Risk Based Validation tool or Jira Align.
Technical thought leadership and the ability to communicate complex technical subjects in business terms.
Experience with DevOps, Continuous Integration, and Continuous Delivery methodologies.
SAFe for Teams certification.
Culture & Benefits
Flexible work arrangements in a Lisbon-based hybrid workplace.
Opportunities to learn, develop, and progress across the global organization.
Diverse and inclusive community where colleagues are empowered to contribute ideas, take risks, and act.
hirify.global Total Rewards Plan including healthcare, financial, wealth, and career benefits.
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