Proclinical Group is seeking a GCP QA Consultant to support quality assurance activities for oncology-focused phase 2-3 clinical trials. The role emphasizes risk management, ICH-GCP compliance, and inspection readiness, collaborating with cross-functional teams to ensure study quality and transparent communication between clinical operations and QA.
The candidate will develop and oversee QA plans, manage site audits, and mentor other QA professionals while working with Regulatory Affairs on
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GCP QA Lead – Oncology Trials (Inspection-Ready) employer: Proclinical Group
Join a globally recognised biopharmaceutical organisation that is at the forefront of innovative therapies, where your passion for protein science and biologic drug development can truly make a difference. With a strong commitment to employee growth, you will thrive in a collaborative work culture that values scientific excellence and offers opportunities to contribute to life-changing therapies. Located in a dynamic environment, this role not only provides hands-on laboratory experience but also fosters professional development through cross-functional teamwork and cutting-edge research.
