Senior Clinical Scientist

Job summary

Are you an experienced Clinical Scientist ready to lead innovation in cancer genomics? Are you passionate about personalised medicine and want to shape the future of genetic testing for cancer susceptibility? Join us at The Royal Marsden and take your career to the next level.

We are looking for an HCPC-registered Senior Clinical Scientist with strong interpersonal and teamworking skills to lead the delivery of germline projects within our Clinical Genomics department. This is a fantastic opportunity to work at the forefront of molecular diagnostics in a world-renowned centre of excellence.

Join the Pioneers at Royal Marsden's Clinical Genomics Lab

The Clinical Genomics laboratory at the prestigious Royal Marsden is at the forefront of innovation and research in the North Thames Genomic Laboratory Hub. As one of the seven national Genomic Laboratory Hubs in England, we're leading the way in Cancer Genomic testing.

Main duties of the job

The post holder will offer a high level of scientific and clinical knowledge, expertise, and skill to provide a high-quality and efficient service in Clinical Genomics. They will be responsible for the variant interpretation and reporting of specialised clinical genomics investigations in cancer susceptibility, haematological and solid tumours and for reporting whole genome sequencing results.

They will be expected to lead and develop the cancer susceptibility section, including designing and implementing new tests for personalised cancer medicine. The post holder will be expected to contribute to the provision of a timely and efficient Clinical Genomics service.

Other key activities include monitoring and reporting key performance indicators, training staff in variant interpretation and reporting complex WGS/NGS results and supervision of staff, as well as contributing to the quality management of the department to ensure continuity of service and compliance with professional standards. The post will involve integrated work with the translational team of the department.

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.

1. Management

Supervise and take responsibility for the day-to-day planning and coordination of the designated clinical area/section of the department, adjusting plans as necessary to ensure continuity of the service. This will include all aspects of the clinical, scientific & technical work, staff management, equipment and quality system as directed. To report to the Head of Clinical Genomics regularly To ensure the timely and efficient provision of core and technologically complex analytical/diagnostic services.

2. Service Delivery

To be responsible for a high-quality Clinical Genomics service focussed on improving patient outcomes. To ensure that clinical requests are met according to agreed policies on the availability of tests and priorities. To ensure that work is carried out in line with Standard Operational Procedures and/or Departmental policy. To be able to work within all relevant areas of the department without or with minimum supervision. To be competent with using both scientific and office-based computer software. To use molecular genetics software packages for the collection and manipulation of data To plan, conduct analyses, and report on highly complex tests performed.

Job description
Job responsibilities

For further information on this role, please see the attached detailed Job Description and Person Specification.

1. Management

Supervise and take responsibility for the day-to-day planning and coordination of the designated clinical area/section of the department, adjusting plans as necessary to ensure continuity of the service. This will include all aspects of the clinical, scientific & technical work, staff management, equipment and quality system as directed. To report to the Head of Clinical Genomics regularly To ensure the timely and efficient provision of core and technologically complex analytical/diagnostic services.

2. Service Delivery

To be responsible for a high-quality Clinical Genomics service focussed on improving patient outcomes. To ensure that clinical requests are met according to agreed policies on the availability of tests and priorities. To ensure that work is carried out in line with Standard Operational Procedures and/or Departmental policy. To be able to work within all relevant areas of the department without or with minimum supervision. To be competent with using both scientific and office-based computer software. To use molecular genetics software packages for the collection and manipulation of data To plan, conduct analyses, and report on highly complex tests performed.

Person Specification

Qualifications

Essential

• HCPC registration as a Clinical Scientist
• MSc/PhD or equivalent in molecular diagnostics/genetics
• Evidence of CPD and relevant training

Experience

Essential

• Significant post-registration experience in molecular diagnostics/genetics
• Experience in cancer susceptibility testing and variant interpretation (germline & somatic)
• Experience with NGS/WGS data analysis
• Experience writing and authorising clinical reports
• Knowledge of ISO 15189, IQA/EQA and audit processes

Desirable

• Senior-level experience in a clinical diagnostic lab

Skills

Essential

• Strong written and verbal communication skills
• Ability to present findings clearly to diverse audiences
• Competent in using lab and data analysis software (e.g., variant interpretation tools, MS Office)
• Analytical, detail-focused and able to troubleshoot complex issues
• Able to plan and manage own workload and supervise others

Person Specification
Qualifications

Essential

• HCPC registration as a Clinical Scientist
• MSc/PhD or equivalent in molecular diagnostics/genetics
• Evidence of CPD and relevant training

Experience

Essential

• Significant post-registration experience in molecular diagnostics/genetics
• Experience in cancer susceptibility testing and variant interpretation (germline & somatic)
• Experience with NGS/WGS data analysis
• Experience writing and authorising clinical reports
• Knowledge of ISO 15189, IQA/EQA and audit processes

Desirable

• Senior-level experience in a clinical diagnostic lab

Skills

Essential

• Strong written and verbal communication skills
• Ability to present findings clearly to diverse audiences
• Competent in using lab and data analysis software (e.g., variant interpretation tools, MS Office)
• Analytical, detail-focused and able to troubleshoot complex issues
• Able to plan and manage own workload and supervise others

Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship

Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the .

From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. .
UK Registration

Applicants must have current UK professional registration. For further information please see

Additional information
Disclosure and Barring Service Check

This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship

Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the .

From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. .
UK Registration

Applicants must have current UK professional registration. For further information please see

Employer details

Employer name

The Royal Marsden NHS Foundation Trust
Address

The Royal Marsden Sutton

Downs Road

Sutton

SM2 5PT

Employer's website