Senior Clinical Data Manager Ii

AstraZeneca

Hybrid
Minimum 5 years clinical data management experience
Experience with edc systems and query management
Knowledge of good clinical data management practices
AstraZeneca is seeking a Senior Clinical Data Manager II to coordinate Clinical Data Management deliverables for clinical studies. The ideal candidate should have a strong background in Clinical Data Management, leadership abilities, and a commitment to collaboration in a hybrid work environment that prioritizes patient care and sustainability

Job Summary

  • This role involves coordinating Clinical Data Management deliverables on assigned studies while acting as the primary point of contact for DM vendors.
  • The successful candidate will demonstrate leadership by overseeing day-to-day operational aspects, identifying risks, and ensuring compliance with regulatory requirements.
  • AstraZeneca offers a collaborative culture with flexible working arrangements that include face-to-face office engagement three days a week.

Matching Summary

Match Score: 85

AstraZeneca is seeking a Senior Clinical Data Manager II to coordinate Clinical Data Management deliverables for clinical studies. The ideal candidate should have a strong background in Clinical Data Management, leadership abilities, and a commitment to collaboration in a hybrid work environment that prioritizes patient care and sustainability.

Skills & Requirements

Must-have

  • Minimum 5 years Clinical Data Management experience
  • Experience with EDC systems and query management
  • Knowledge of Good Clinical Data Management Practices
  • Ability to work in a global team environment

Nice-to-have

  • Experience leading clinical studies as Data Management Lead
  • Understanding of CDISC data standards and practices
  • Knowledge of SQL or SAS software tools
  • Willingness to mentor junior colleagues

Key Requirements

  • University degree in life sciences or related field
  • Minimum 5 years of CDM experience in Biotech/Pharma/CRO
  • Demonstrated understanding of GCDMP and regulatory requirements

Work Rights

Not specified

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