25 Mar
Associate Research Operations
California,

Day to Day Responsibilities:



  • work with oncology department (regulatory submission, data verification background)


  • Ensure consistency and compliance with report writing and ELN documentation procedures

  • Conduct formal QC review and data verification of nonclinical research study reports and related ELNs, and other regulatory documents

  • Participate in the development and alignment of QC timelines for regulatory documents and preparation of assigned deliverables

  • May collaborate with external contractors and contracted research organization (CRO) vendors on QC related matters

  • Potential opportunity to serve as ICH Module 4 nonclinical study report coordinator (based upon performance and/or functional area need)


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