Manager Of Gcp Auditing

in Healthcare + Life Sciences
  • Boston, Massachusetts View on Map
  • Salary: $135,000.00 - $149,000.00
Permanent

Job Detail

  • Experience Level Manager
  • Degree Type Bachelor of Science (BS)
  • Employment Full Time
  • Working Type Hybrid
  • Job Reference 0000018345
  • Salary Type Annually
  • Industry Pharmaceuticals
  • Selling Points

    Lead impactful GCP auditing processes and ensure regulatory compliance excellence. Collaborate with cross-functional teams to resolve compliance issues effectively. Gain valuable experience in clinical quality assurance leadership.

Job Description

Overview

  • Manage clinical quality assurance (CQA) processes, ensuring compliance with Good Clinical Practices (GCP) and regulatory standards.
  • Conduct audits for clinical sites, vendors, and internal systems to maintain quality standards.
  • Collaborate with cross-functional teams to resolve compliance issues and implement corrective actions.
  • Support clinical development activities through vendor qualification and document audits.
  • Provide training and guidance on GCP standards to internal teams and external collaborators.
  • Develop and oversee audit plans, ensuring alignment with organizational goals and regulatory requirements.
  • Maintain audit tracking systems and report metrics to management.
  • Assist in regulatory inspections and ensure readiness for compliance evaluations.

Key Responsibilities & Duties

  • Conduct and supervise GCP audits for clinical vendors, sites, and documents.
  • Collaborate on deviation management activities, including root cause analysis and CAPA development.
  • Plan and execute GLP and GCP vendor audits, ensuring compliance with standards.
  • Review audit reports and ensure corrective actions meet regulatory requirements.
  • Provide GCP training for clinical investigator meetings and internal teams.
  • Collaborate with clinical development teams to resolve audit findings and improve practices.
  • Maintain tracking systems for audit activities and provide periodic metrics reports.
  • Assist in regulatory inspections and prepare documentation for compliance evaluations.

Job Requirements

  • Bachelor’s degree in Nursing, Health Science, or a related field.
  • Minimum of 8 years of experience in clinical auditing and compliance.
  • Proficiency in GCP auditing, including clinical reports, investigational sites, and vendor audits.
  • Knowledge of US and ICH GCP regulations and guidelines.
  • Experience with clinical safety and trial management systems like ARISg and TrackWise.
  • Strong interpersonal, oral, and written communication skills.
  • Ability to prioritize tasks, manage competing timelines, and work independently or collaboratively.
  • Willingness to travel 40-60% for audits and inspections.
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