About
IQVIA Laboratories is a global leader in drug discovery and development laboratory services, offering a comprehensive suite of central laboratory and specialty biomarker services. Our expertise spans genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine assays, vaccine assays, ADME, and bioanalytical services.
We specialize in antibody and biomarker discovery, as well as decentralized clinical trial laboratory solutions. Committed to scientific rigor and operational excellence, we support every phase of the drug development and discovery process across diverse regions and regulatory frameworks, ensuring the highest standards of data integrity and accelerating the delivery of transformative therapies to patients.
The position is located on-site at the IQVIA Laboratories facility in Livingston, within easy commuting distance from Edinburgh, Glasgow, and other beautiful Scottish tourist attractions.
Job Overview:
Clinical trials are essential for medical advances, including precision medicine. You will work at the cutting edge of treatment development in various malignancies, using histopathology, immunohistochemistry, and fluorescent in-situ hybridisation for diagnostic and biomarker assessment.
This role offers a unique opportunity to improve quality of life for patients with acute and debilitating conditions.
The post consists of 10 programmed activities, with an initial appointment to 9 DCC and 1 SPA. There is no on-call commitment.
No surgical cut-up, gynae cytopathology, or autopsy work is required.
You will support daily operations in laboratories to deliver sponsor requests and studies, overseeing technical processes and procedures that impact pathology interpretations.
Timely reports will be released into LIMS for sponsor and/or clinical site action.
Requirements:
* Medical Degree (Doctor of Medicine, or foreign equivalent)
* Full Registration with a Licence to Practise from the General Medical Council Fellowship of The Royal College of Pathologists (or equivalent) and a minimum of 2 years' experience of independent reporting practice. Placement on the Specialist Register of the GMC is required.
Benefits of joining us:
* A career-enhancing opportunity to work at the forefront of treatment development in various malignancies, joining an existing team of consultants.
* Work-Life Balance with a focus on positive well-being.
* Continuous career development and growth opportunities.
* Variety of therapeutic areas.
* A collaborative and supportive team environment.
* Access to innovative in-house technology.