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описание
IQVIA provides clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Its ClinSpark platform is a CDISC ODM certified eSource and clinical trial automation system that supports device integrations and improves the speed, quality, and transparency of clinical research.
задачи
Lead efforts to gather, analyze, define, document, and validate software requirements;
Define requirements for core web application functions, system and device integrations, data visualization, and reporting capabilities;
Work with key stakeholders to understand challenges and determine needs versus wants;
Learn, understand, and document product functionality and capabilities;
Drive effective planning, reporting, and analysis for internal functions;
Create and contribute to technical product documentation supporting SDLC, including software design documents, functional specifications, and change requests;
Create diagrams and other visual assets to depict capabilities and workflows when needed;
Perform systems analysis at the highest technical level across most phases while considering the impact of technology on the current and future business environment.
требования
Minimum five years of related systems or business analysis experience;
Knowledge of software development processes and best practices;
Ability to work independently in a remote team environment;
Strong technical skills and experience working within software development teams;
Experience with Software Development Life Cycle (SDLC) methodologies;
Experience with BDD methodologies and requirement definition;
Strong analytical and problem-solving skills;
Excellent written, verbal, communication, and interpersonal skills;
Detail-oriented with excellent time management and organizational skills;
Ability to understand client requirements and the underlying infrastructure, applications, systems, and processes needed to execute them;
Nice to have: Bachelor's Degree in Computer Science or Business Administration or equivalent experience, experience with Atlassian systems including Jira and Confluence, knowledge of business-wide applications or IQVIA client-facing applications and products, knowledge of Phase I-IV clinical trial operations and workflows, expertise in clinical trial management software, knowledge of applicable clinical research, regulatory, and other requirements including Good Clinical Practice, HIPAA, GDPR, EMA, GAMP5, and FDA 21 CFR Part 11.