Senior Clinical Data Manager Ii

AstraZeneca

**
Minimum 5 years clinical data management experience
Experience with good clinical data management practices
Proficiency in electronic data capture systems
** AstraZeneca is seeking a Senior Clinical Data Manager II to oversee Clinical Data Management deliverables for clinical studies, ensuring compliance with standards and regulations. The role emphasizes collaboration, leadership, and effective communication within a hybrid work environment that values employee flexibility and teamwork. **

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 position requires maintaining business continuity for CDM processes and ensuring the integrity of the clinical database for relevant studies.
  • Candidates will collaborate with a global team to drive adherence to AstraZeneca CDM standards and manage vendor performance against KPIs.

Matching Summary

Match Score: 75

** AstraZeneca is seeking a Senior Clinical Data Manager II to oversee Clinical Data Management deliverables for clinical studies, ensuring compliance with standards and regulations. The role emphasizes collaboration, leadership, and effective communication within a hybrid work environment that values employee flexibility and teamwork. **

Skills & Requirements

Must-have

  • Minimum 5 years Clinical Data Management experience
  • Experience with Good Clinical Data Management Practices
  • Proficiency in electronic data capture systems
  • Strong query management and reconciliation skills
  • Ability to work in a global team environment

Nice-to-have

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

Key Requirements

  • University degree in life sciences, pharmacy, nursing, or equivalent
  • Minimum 5 years of experience in Biotech/Pharma/CRO industry
  • Demonstrated understanding of regulatory requirements and GCDMP

Work Rights

Not specified

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