This is a temporary role to cover maternity leave absence for one of our existing Clinical Project Managers. The Clinical Project Manager is responsible for managing our Neumifil clinical program as an influential, capable and credible project management professional. Reporting to the CEO, the Clinical Project Manager has accountability for the clinical programs to progress on time and budget. The individual contributes to creating a safe working environment, and an inclusive, agile and collaborative culture for the Pneumagen employees and consultants as well as maintaining robust and constructive relationships with service providers to the Company. Responsibilities Project Management The Clinical Project Manager position is in the Development Group of Pneumagen Limited. The post-holder will provide high-level project management skills for managing and delivering the clinical aspects of Pneumagen’s lead program. · Ensure that the clinical development plan (objectives and timelines) is clearly communicated and understood by all required parties. · Working with the CEO, CMO and the function leads / subject matter experts to develop, agree and deliver a detailed clinical development plan aligned to the Company’s development goals. · Support the function leads in the generation of clinical Request for Proposals and clinical contractor selection. · In co-ordination with the function leads and CEO, manage the Company’s relationship with its clinical trial CROs · Contribute to the overall scientific excellence of the development activities. Core Responsibilities · Provide CRO and vendor management of assigned clinical trials · Management of day-to-day operations of assigned clinical trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. · Serve as main point of contact for assigned clinical trials, for both internal and external study stakeholders, ensuring effective communication and collaboration skills · Draft and review clinical project plans and manage key clinical trial documentation for assigned clinical trials as well as identifying appropriate members of the team to also review. · Provide regular scheduled and ad hoc updates of clinical development activities to Project Team, CEO and key stakeholders including updating the Clinical Development Plan · Manage study deliverables and track study metrics including identifying potential risks to study timelines and deliverables · Chair, coordinate and minutes the clinical team meetings as necessary including risk and issue management, and clinical strategy meetings. · Monitor clinical budgets and attend frequent forecast meetings. · Develop and maintain Gantt charts for assigned clinical trials · Coordinate sponsor sign-off and filing of clinical trial documents. Qualifications · Bachelor's degree or higher in relevant field · Significant experience in clinical trial management and knowledge of GCP, ICH guidelines and other clinical regulatory requirements · Strong interpersonal, organisational and prioritisation skills, able to communicate at multiple levels of organization