Medical Laboratory Coordinator

2 weeks ago

Sutton Coldfield, Birmingham, United Kingdom The Royal Marsden Full time
Job Overview

The Royal Marsden is seeking a highly organized and detail-oriented individual to join our team as a Medical Laboratory Coordinator. This role will play a critical part in the future of our Integrated Pathology Unit, as we navigate the integration of artificial intelligence and digitization of pathology material.

Main Responsibilities
  • Coordinate and facilitate access to clinical images, biomaterials, and metadata for individual projects initiated by RMH or ICR scientists.
  • Monitor the use of clinical images, biomaterials, and metadata in individual projects.
  • Support the creation of documentation required for each study, related to access to clinical images, biomaterials, and metadata.
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), and retrospective translational research projects.

  • Work with IPU leadership to create a robust and efficient pipeline to coordinate and facilitate access to clinical images, biomaterials, and metadata.
  • Coordinate, navigate, and facilitate all regulatory internal requirements, including:
    • Medicines for Human Use (Clinical Trials) Regulations
    • Research Governance Framework for Health and Social Care
    • Human Tissue Act
    • Research and Development Policies and SOPs
  • 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 organized 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 consult where appropriate.
  • Ensure that all Trust and IPU policies and standard operating procedures are adhered to.
Person Specification

The ideal candidate will possess:

  • A life sciences degree or equivalent.
  • Well-developed IT and internet skills.
  • Competence in research-oriented PC software, including databases, Excel, and SPSS.
  • Evidence of Continuing Professional Development.

Desirable criteria include:

  • Postgraduate or higher-level education equivalent in a relevant area.
Experience

The successful candidate will have:

  • Experience in translational/clinical project coordination or working in a clinical research environment.
  • Detailed understanding and experience of clinical studies, including operational aspects and regulatory framework.
  • Experience in clinical data collection, curation, and maintenance.
Special Aptitude & Disposition

The ideal candidate will possess:

  • Advanced organizational skills and ability to manage multiple projects at various stages of development and organization.
  • Excellent cross-disciplinary/interagency communication skills and ability to facilitate collaborative working relationships.
  • Confident and articulate with excellent written and oral communication skills.
  • Ability to make decisions and prioritize effectively.
  • Ability to innovate and respond to change.
  • Independent and able to work unsupervised.

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