QA Auditor II
About the role
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- Effectively plan and conduct regular and random internal and external, QA Audits in order to assure that clinical studies managed by ICON are of the highest standard and are in compliance with the requirements of ICON or Sponsor SOP’s, study protocols, relevant regulations and guidelines and with ISO 9000 requirements.
- Preform quality system audits if required.
- Preform contract audits for Sponsor companies are required.
- Ensure that audit results are formally recorded and reported and that corrective/ preventative actions are documented.
- When appointed lead auditor, perform the duties assigned in an efficient and effective manner. This includes liaison with the project manager on all QA issues, including audit planning and review of audit results.
- Assist with the development of the project audit procedures.
- Assist in training new QA auditors.
- Assist in training ICON staff regarding GCP, ISO 9000, role of QA, regulatory inspections etc.
- Conduct induction/ orientation of new staff in ICON quality policies and procedures.
- Assist with business development activities (such as marketing presentations) when appropriate.
- Provide a benchmark of auditing competencies to inexperienced colleagues.
- Assume additional QA responsibilities as directed by QA manager.
- Keep the person whom the QA auditor reports to informed of any QA issues within the department that require attention.
- Travel is approximately 35%
- Bachelor’s Degree or local equivalent in medicine or science.
- Background in medicine, science and/ or other relevant discipline and appropriate experience.
- Previous experience in Quality Assurance auditing and/or 2-3 years of proven clinical research experience.
- Detailed knowledge of GCP guidelines and relevant regulations for the conduct of clinical trials.
- Ability to review and evaluate clinical data/ records.
- Excellent communication and interpersonal skills.
- Ability to successfully implement quality plans for specific phases of a trial.
- Ability to liaise with project teams.
- Good understanding of drug development and clinical trial process.
Application process
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