Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Digital Medicine and Translational Imaging - FSP
Job ID R0000039817 , United KingdomResponsibilities:
• Participate and contribute to the development of operational plans to ensure data quality
and completeness
• Develop, Implement, and Conduct data quality checks as needed for work/studies
• Contribute technical expertise toward the design, implementation, and scaling up of
sensor systems and analytics
• As a medical informaticist, ensure collection, organization, curation, storage and
safeguarding of patient data, asset teams, and external collaboration
studies is consistent with 21CFR part 11
• Contribute to the overall architecture of the existing data pipelines and workflows,
recommends and implements improvements
• Track emerging study data and works closely with data science team to ensure the
effectiveness of tools and data quality
• Manage own time to meet agreed targets
• Work under general supervision. Performs assignments using established procedures
and general instruction
• Share learnings with key stakeholders and the scientific community through
presentations and peer-reviewed publications.
Minimum Qualifications:
• Master’s degree in Health Informatics, Computer Science, Information Systems, or similar field
• A minimum of 5+years of technical experience, including:
• Python
• Unix/Linux environments
• Version control systems (ex. Git)
• AWS or other cloud-based development
• Electronic data captures (EDC) solutions, e.g., REDCap, Encapsia, Oracle Clinical,
Medidata Rave
• Familiarity with pharmaceutical informatics standards like CDISC and MedDRA
• GCP
• Strong interpersonal and collaboration skills
• Demonstrate the ability to build consensus and be agile to changing circumstances and
priorities
• Hands-on experience with Clinical Data Management, including Case Report Form (CRF)
design, CRF annotation, database design, data collection, data-entry, data validation,
discrepancy management, medical coding, data extraction, database locking, and
regulatory requirements
Preferred Qualifications:
• Clinical trial experience using and deploying digital health technologies
• Experience with electronic data captures (EDC) solutions, e.g., REDCap, Medrio
• Familiarity with medical informatics standards like CDISC
• Experience with AWS or other cloud-based development
• Experience processing large data sets (including from digital health technologies) in a
distributed computing environment
• Experience with SQL or NoSQL-based technologies
• Comprehensive understanding of the landscape of data structures, medical ontologies,
interoperability standards, and data processing tools
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