Senior QA Auditor (GCP)

Description

Drive clinical excellence as the guardian of GCP integrity and audit quality.

R&D Partners is seeking a Senior QA Auditor with expertise in Good Clinical Practice (GCP). This role focuses on ensuring compliance with regulatory standards and maintaining quality assurance within clinical research processes.

This is a fully remote role based anywhere in North America.

Applicants must have legal authorization to work in the United States.

Responsibilities:

• Conduct audits to ensure adherence to GCP guidelines and regulatory requirements.
• Collaborate with cross-functional teams to identify and resolve compliance issues.
• Develop and implement quality assurance strategies and processes.
• Provide training and guidance on GCP standards to internal teams.
• Prepare detailed audit reports and follow up on corrective actions.

Key Skills and Requirements:

• Proven experience in Quality Assurance with a focus on GCP.
• Strong knowledge of regulatory requirements and industry standards.
• Excellent communication and organizational skills.
• Ability to work independently and manage multiple priorities.
• Relevant certifications or qualifications in clinical research or quality assurance are preferred.

For more information, please contact Jacob Tutt.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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