Position: Mid-Senior level

Job type: Full-time

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Job content

Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions – underpinned by the world’s largest delivery network – Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 469,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com.

Job Description-

  • Understanding and experience of the Clinical and Regulatory Pharma R&D domains and systems landscape

  • A good understanding and awareness of the overall components of large transformation programs in Regulatory and Clinical, and deep expertise in either of these areas: Business process design, process mapping, data strategy and data flows, test and validation, migration preparation, change management and training

  • Experience and understanding of cloud solutions for Clinical and Regulatory systems (e.g., RIM, CTMS, eTMF, SSU etc.)

  • Experience and understanding of implementing solutions in an agile fashion and related ways of working (SAFe, Scrum, Kanban, etc.)

  • Experience working with colleagues and stakeholders across multiple functions, grades, geographies, and time zones

  • Ability to understand an emerging regulation and decipher the related data, functionality, system, and integration requirements

  • Leading and participating in clinical and regulatory business process discussions, identifying requirements and user stories

  • Authoring high-level user stories and develop related tasks, acceptance criteria and test cases

  • Leading workshops with businesses for prioritising user stories for further development

  • Work with Business Consultants from functional areas to support configuration of requirements, relationships, the building of cross-links etc. to build required fields, features, and metadata/data exchange between platforms

  • Support architecture and development teams with solution design, application integration and data exchange design requirements

  • Building client proposal that details the required technical solution, resourcing costs and budget to support client organisation endorsement and programme funding approval

  • Good to have-

  • Understanding of the Pharma R&D Clinical and Regulatory value chain and related processes

  • Experience with building solutions for regulatory compliance, preferably compliance for a new pharma regulation and delivering compliance for large enterprise programmes

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    Deadline: 08-04-2024

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