Job summary
With the scope of digital pathology, pathologists are now able to convert glass slides of patients' tissue samples into digital slides that can be viewed and analysed on a computer. The Integrated Pathology Unit (IPU) runs one of the most advanced translational digital pathology operations in Europe and bridges the gap between science and patients within the scope of digital pathology, tissue hybridization and artificial intelligence (AI) technologies. The IPU represents an opportunity to make a substantial impact to the way we understand, diagnose and characterize cancer. The IPU works with teams at The Royal Marsden, the ICR, international and national collaborators, research organizations and commercial partners. This role plays a key part in the future of the IPU as we begin to enter a new realm of regulatory compliance with applications of AI and digitisation of pathology material, and multimodal analysis. As these techniques become the new norm, we need to ensure they are seamlessly integrated into new study setups and future translational research. The ultimate aim being primarily, to make it easier and quicker to set-up and deliver more complex tissue- and data-driven research. The post holder will be responsible for coordinating and facilitating all the activities required for the effective access to and monitoring of clinical images, biomaterials and meta-data for individual projects initiated by RMH or ICR scientists.
Main duties of the job
The holder of the post is expected to perform a variety of tasks that may include, but are not restricted to:
Responsible for coordinating and facilitating all the activities required for the effective access to clinical images, biomaterials and meta-data for individual projects initiated by RMH or ICR scientists
Monitor the use of clinical images, biomaterials and meta-data in individual projects
Support and actively engage in the creation of the documentation required for each study, in relation to access to clinical images, biomaterials and meta-data in individual projects
About us
The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals - one in Chelsea, London, and one in Sutton, Surrey - as well as a Medical Daycare Unit in Kingston Hospital.
At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.
At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.
Job description
Job responsibilities
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
Person Specification
Attainments
Essential
1. Life sciences (or equivalent) degree
2. Well-developed IT (Microsoft Work package) and internet skills
3. Competence in research orientated PC software (Databases, Excel, SPSS)
4. Evidence of Continuing Professional Development.
Desirable
5. Postgraduate or higher level education equivalent in relevant area
Experience
Essential
6. Experience in translational/clinical project coordination or working in a clinical research environment
7. Detailed understanding and experience of clinical studies, including operational aspects and regulatory framework
8. Experience in clinical data collection, curation and maintenance
Special Aptitude & Disposition
Essential
9. Advanced organisational skills and ability to manage multiple projects at various stages of development & organisation
10. Excellent cross-disciplinary/interagency communication skills and ability to facilitate collaborative working relationships
11. Confident and articulate with excellent written and oral communication skills
12. Ability to make decisions and prioritise effectively
13. Ability to innovate and respond to change
14. Independent and able to work unsupervised