Digital Medicine and Translational Imaging - FSP
Masters
Description
<p><b>When our values align, there's no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.</p><p></p><p></p><p><b>Responsibilities:</b></p><p></p><p>• Participate and contribute to the development of operational plans to ensure data quality</p><p>and completeness</p><p>• Develop, Implement, and Conduct data quality checks as needed for work/studies</p><p>• Contribute technical expertise toward the design, implementation, and scaling up of</p><p>sensor systems and analytics</p><p>• As a medical informaticist, ensure collection, organization, curation, storage and</p><p>safeguarding of patient data, asset teams, and external collaboration</p><p>studies is consistent with 21CFR part 11</p><p>• Contribute to the overall architecture of the existing data pipelines and workflows,</p><p>recommends and implements improvements</p><p>• Track emerging study data and works closely with data science team to ensure the</p><p>effectiveness of tools and data quality</p><p>• Manage own time to meet agreed targets</p><p>• Work under general supervision. Performs assignments using established procedures</p><p>and general instruction</p><p>• Share learnings with key stakeholders and the scientific community through</p><p>presentations and peer-reviewed publications.</p><p></p><p><b>Minimum Qualifications:</b></p><p>• Master’s degree in Health Informatics, Computer Science, Information Systems, or similar field</p><p>• A minimum of 5+years of technical experience, including:</p><p>• Python</p><p>• Unix/Linux environments</p><p>• Version control systems (ex. Git)</p><p>• AWS or other cloud-based development</p><p>• Electronic data captures (EDC) solutions, e.g., REDCap, Encapsia, Oracle Clinical,</p><p>Medidata Rave</p><p>• Familiarity with pharmaceutical informatics standards like CDISC and MedDRA</p><p>• GCP</p><p>• Strong interpersonal and collaboration skills</p><p>• Demonstrate the ability to build consensus and be agile to changing circumstances and</p><p>priorities</p><p>• Hands-on experience with Clinical Data Management, including Case Report Form (CRF)</p><p>design, CRF annotation, database design, data collection, data-entry, data validation,</p><p>discrepancy management, medical coding, data extraction, database locking, and</p><p>regulatory requirements</p><p></p><p><b>Preferred Qualifications:</b></p><p>• Clinical trial experience using and deploying digital health technologies</p><p>• Experience with electronic data captures (EDC) solutions, e.g., REDCap, Medrio</p><p>• Familiarity with medical informatics standards like CDISC</p><p>• Experience with AWS or other cloud-based development</p><p>• Experience processing large data sets (including from digital health technologies) in a</p><p>distributed computing environment</p><p>• Experience with SQL or NoSQL-based technologies</p><p>• Comprehensive understanding of the landscape of data structures, medical ontologies,</p><p>interoperability standards, and data processing tools</p><p></p>