Parexel

Medical Informatics Manager – Digital Medicine Study Manager

Parexel

full-time

Posted on:

Location Type: Remote

Location: United Kingdom

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About the role

  • Responsible for mapping local study dictionaries sponsor standards
  • 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
  • Work closely with the various stakeholders to understand evolving project portfolio needs, and integration into the systems and requirements; supporting studies with a wide range of disease domains.
  • Contribute technical expertise toward the design, implementation, and scaling up of sensor systems and analytics
  • Ensure collection, organization, curation, storage and safeguarding of patient data
  • 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.

Requirements

  • Master’s degree in Health Informatics, Computer Science, Information Systems, or similar field
  • A minimum of 5+ years of technical experience
  • 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
  • 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.
Benefits
  • 100% homebased position
  • Professional development opportunities
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
PythonUnix/LinuxVersion control systemsAWSElectronic data captureClinical Data ManagementCase Report Form designData validationMedical codingDatabase design
Soft Skills
Interpersonal skillsCollaboration skillsAgilityConsensus buildingTime management