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Product Owner

icon building Company : Remarque
icon briefcase Job Type : Full Time

Number of Applicants

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Job Description - Product Owner

Remarque Systems is looking for a Product Owner to join our Clinical Technologies team.

Remarque Systems is a clinical technology company that is passionate about improving drug development using cutting edge software. Remarque is designed to simplify study management and propel innovation by consolidating data and support strategic decision making. 

What you'll be doing:

  • Become the subject matter expert for the Remarque Systems Platform as a whole.

  • Work closely with internal and external customers to translate the platform vision into detailed requirements.

  • Work with internal and external customers to understand business needs and prioritize product backlog.

  • Work with senior management and architects on overall flow of products to align business need with architectural vision.

  • Work with developers to create simulations and user interface designs as required.

  • Consult with Product Testing team to ensure testing is delivering a solid platform.

  • Be comfortable demonstrating and explaining platform to internal and external customers.

  • Work with project management to ensure all deliverables meet needs for release documentation.

  • Work with training and support functions to ensure a smooth handover of new functionality.

  • Create release notes for new functionality to be shared with internal and external customers.

What we are looking for:

  • Bachelor’s degree in computer science, information systems, engineering or related discipline, or equivalent combined education and experience.

  • Ability to focus on customer excellence.

  • 7+ years of experience in information technology with at least 5 years focused in life sciences.

  • Experience with large-scale software implementations.

  • Excellent analytical and problem-solving skills.

  • Excellent documentation skills.

  • Excellent customer service skills.

  • Experience with the clinical trial industry and processes.

  • Familiarity with computer systems validation.

  • Familiarity with Food and Drug Administration and ICH/GCP guidelines.

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