We are seeking an enthusiastic, self-motivated Clinical Scientist with experience in molecular diagnostics to contribute to the provision of a timely and efficient ISO 15189 accredited Clinical Genomics Service. The post holder will be responsible for testing and reporting specialised molecular diagnostics investigations, including contributing to the ctDNA workflow in collaboration with Guardant. They will be involved in service development and validation, including implementing new tests for personalised cancer medicine and analysis using complex genetics software. Additionally, the post holder will support activities such as quality management, compliance with laboratory accreditation standards, training, and the department’s translational research programme. Good communication, team working, and supervisory skills are essential.
The successful applicant should hold an MSc in a biological science (or equivalent) and be HCPC registered as a Clinical Scientist. Ideally, they will have substantial experience in molecular diagnostics service delivery and a solid understanding of molecular techniques, with experience in high throughput sequencing technologies, analysis, and variant interpretation being desirable.
Main duties of the job
The main objective is to contribute to the provision of a timely and efficient Molecular Diagnostics service within the Clinical Genomics Department for both internal and external cases. The post holder will perform analysis using complex genetics software, report specialised molecular investigations, and manage existing service work to ensure high-quality molecular diagnostic services in haematological and solid tumours. The range of tests will continually evolve, and the post holder will be responsible for standardising new technologies and tests. They will liaise with clinicians, oncologists, and histopathologists involved in patient care.
Detailed job description and main responsibilities
1. Ensure work complies with Standard Operating Procedures and departmental policies.
2. Prioritise daily work and coordinate service provision with users.
3. Supervise the allocation of duties to junior scientists and medical laboratory assistants.
4. Participate in the preparation and review of SOPs and protocols.
5. Adhere to the Departmental Health and Safety Policy and conduct risk assessments as needed.
6. Maintain accurate records of laboratory activities, including equipment maintenance, reagent usage, and troubleshooting.
7. Maintain patient confidentiality in accordance with HCPC and Information Governance guidelines.
Person specification
Skills and Abilities
* Experience in clinical report writing
* Clear and concise communication skills
* Experience with complex genetics software
* Proficiency in Microsoft Office or equivalent
Personal Qualities
* Commitment to personal development
* Self-confidence and active participation in team meetings
* Ability to work independently
* Flexible approach and decision-making skills
Specific Experience
* MSc degree or equivalent experience
* Relevant training and continuous professional development
* Experience in diagnostic laboratory operations
* Ability to write, review, and follow SOPs
* Experience with advanced training and compliance with standards
* HCPC registration (essential)
* Experience with NGS for diagnostics or clinical trials
* Stock management skills
* Ability to manage laboratory areas and staff daily
The Royal Marsden values diversity and encourages applications from underrepresented groups, including Black, Asian, minority ethnic candidates, LGBTQ+ candidates, and those with disabilities.
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