Integrated Research Manager
2 months ago
For further information on this role, please see the attached detailed Job Description and Person Specification: Service Delivery.....
For further information on this role, please see the attached detailed Job Description and Person Specification: Service Delivery: The Integrated Pathology Unit will oversee and contribute to a wide range of projects, clinical trials and RM/ICR led academic studies. This may include multicentre trials, UK Clinical Trials of Investigational Medicinal Product (CTIMP) to retrospective translational research projects. The potholder will: 1. Work with IPU leadership to create a strong, robust and efficient pipeline to coordinate and facilitate all the activities required for the effective access to clinical images, biomaterials and meta-data for individual projects initiated by RMH or ICR scientists 2. Coordinate, navigate and facilitate all regulatory internal requirements including (when applicable): a. Medicines for Human Use (Clinical Trials) Regulations b. Research Governance Framework for Health and Social Care c. Human Tissue Act d. Research and Development Policies and SOPs 3. Be the main point of contact for the clinical R&D Office for set up of assigned R&D projects. General Duties: Work in a flexible, but organised manner Meet objectives within predetermined timescales Communicate effectively with other members of the Centre of Molecular Pathology, the BRC and other Trust staff Work under the supervision of the line manager and to consult where appropriate Ensure that all Trust and IPU policies and standard operating procedures are adhered to
Official account of Jobstore.