Senior/principal Clinical Data Manager

AstraZeneca

Multiple Locations
Not specified
Clinical data management
Gcdmp and regulatory requirements
Clinical databases and edc
AstraZeneca is seeking a Senior/Principal Clinical Data Manager to provide project-level administrative support throughout the clinical study lifecycle. The ideal candidate will have a strong background in clinical data management, excellent organizational skills, and experience with various clinical data systems

Job Summary

  • Provide project level CDM administrative support for study start up, conduct and closeout phases, including documentation review, user access testing, query management, data cleaning, and third-party data reconciliation.
  • Collaborate with Data Management Vendors on deliverables and milestones, oversee data and documentation quality, and identify/mitigate risks in coordination with the Principle Clinical Study Data Manager.
  • Drive adherence to AZ CDM standards and processes for data quality and consistency, maintain awareness of external and internal models for continuous improvement, and mentor junior Clinical Data Management colleagues.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior/Principal Clinical Data Manager to provide project-level administrative support throughout the clinical study lifecycle. The ideal candidate will have a strong background in clinical data management, excellent organizational skills, and experience with various clinical data systems.

Skills & Requirements

Must-have

  • Clinical Data Management
  • GCDMP and regulatory requirements
  • Clinical databases and EDC
  • Query management and reconciliation
  • CDISC data standards
  • SQL, 4GL, VBA or R software

Nice-to-have

  • Mentoring junior colleagues
  • Continuous improvement awareness
  • Global team collaboration
  • Ad hoc activity willingness

Key Requirements

  • University or college degree in life sciences or related subject
  • Experience in Biotech/Pharma/CRO industry
  • Demonstrated understanding of clinical and pharmaceutical drug development process
  • Demonstrated ability to work effectively with external partners

Work Rights

Not specified

Tailored Resume

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