Senior Manager, Clinical Quality Operations

 Posted an hour ago
     
5-10 years experience
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AI Summary

The Senior Manager will oversee quality project management for pre-clinical and clinical programs, ensuring GXP compliance across Clinical, CMC, and Nonclinical teams. This includes maintaining the Quality Management System, managing vendor oversight, and leading audit programs and remediation efforts.

The Senior Manager, Clinical Quality Operations will be responsible for Quality project management of pre-clinical and clinical programs by providing GXP support to Atsena Therapeutics’ Clinical, CMC, and Nonclinical teams through management of documentation review, compliance trending and maintenance of quality issues, and vendor oversight. The Senior Manager, Quality Operations will implement and maintain the Quality Management System (QMS) through quality standards, policies, and procedures, including document management in the Veeva Vault QualityDocs platform. The Senior Manager, Quality Operations will assist in GXP risk assessment activities in collaboration with business stakeholders and ensure compliance with global regulatory, vendor, and internal company quality systems requirements.

 

Responsibilities:

  • Partners with Atsena’s Clinical, CMC, and Nonclinical teams, external vendors, and investigator sites to provide GCP/GXP Quality oversight including assistance in risk assessments and quality oversight initiatives.
  • Collaborates with external vendors; and Atsena Clinical, CMC, and Nonclinical teams to provide GCP/GXP and QA expertise while ensuring project objectives are met in a compliant and timely manner.
  • Assesses compliance of vendors, investigator sites, study activities, etc. with study protocols, SOPs, and ICH and other applicable regulatory requirements.
  • Develops and implements the internal/external GCP/GXP audit program for their clinical program(s), including scheduling, consultant oversight and audit report review and approval.
  • Leads significant Quality issues management system for assigned studies, including assessment of potential root causes and remediation (corrective and preventative actions).
  • Ensures appropriate and timely escalation of quality issues, including potential misconduct or issues of significant deviation, with programs/products to Leadership.
  • Assists and implements initiatives that promote and maintain a quality culture and awareness towards Data Integrity and Good Documentation Practices.
  • Supports GCP/GXP PAI readiness activities by partnering with internal operational and Quality leadership.


 

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