Clinical Research Senior Administrator

For further information on this role, please see the attached detailed

Job Description and Person Specification

Monitor generic emails accounts and return or distribute correspondence to relevant stakeholders. This will include other generic inboxes managed by the governance and operations function. Provide administrative guidance to research project applicants preparing submissions to CCR and DTARS, and signpost to subject matter experts as needed. Arrange internal review and approvals of research applications to ensure that all applications are reviewed to the required standard and in accordance with the ethical and regulatory expectations, including the coordination of costings and contracts for applications. Maintain guidance documents, SOPs and templates, and circulate updates as required to all stakeholders. To be responsible for coordinating and managing the approvals process for modifications (both site and RM/ICR sponsor).