For further information on this role, please see the attached detailed Job Description and Person Specification: To ensure along with the DI that commissioned cellular therapy products and ATIMPs meet regulatory requirements To provide support and expert advice to clinical research teams in meeting Human Tissue Authority (HTA) and JACIE requirements To work under the direction of and to communicate regularly with the Trusts HTA Designated Individual (DI) for the Human Application licence. To keep up-to-date on legislative requirements and make recommendations for subsequent operational changes To ensure full traceability of tissues and cells from collection to infusion or disposal along with the wider quality team.