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Specialist Biomedical Scientist - Blood Sciences

East of England, East of England

Permanent

£35,392 to £42,618

Medical/Clinical Scientist

Job summary

We currently have an exciting opportunity for a Band 6 Specialist Biomedical Scientist to join our Blood Sciences team at The Christie Pathology Partnership. The Christie is the largest single site cancer centre in Europe and the first UK centre to be accredited as a comprehensive cancer centre; with more than 60,000 patients treated a year. This is full-time permanent role and you will be expected to participate 24/7 rota.

Christie Research has more than 650 open trials and is the largest centre in the UK for commercial cancer trials. It is a Cancer Research UK Major Centre, part of the National Institute for Health Research (NIHR) Biomedical Research Centre, and hosts the NIHR Manchester Clinical Research Facility. The Trust is also one of the first wave of hospitals offering CAR-T therapy on the NHS.

Main duties of the job

To be able to rotate through all areas of a Laboratory as required (dependent on qualifications, experience and training), to perform all designated duties in accordance with local working practices, to maintain high Professional standards and conform to Health and Safety regulations

To perform and interpret routine and specialist biomedical investigations autonomously to provide patients results within agreed quality standards of service delivery and turnaround times under the supervision of senior staff

Work independently, implement and propose changes to procedures for own work area. May be a lead specialist

To provide professional leadership and training to Basic Grade, Trainee BMS, Associate Practitioners (equivalent grades) and Medical Laboratory Assistants

To provide specialist technical advice to clinicians as to the appropriateness of tests and timescales

About us

SYNLAB UK & Ireland work closely with clinicians, hospitals, occupational health providers and clinical researchers to provide a complete pathology offering.

We operate in increasingly diverse environments which is reflected in our workforce, clients, customers, suppliers, communities and partners. We believe an inclusive workplace culture is the best way to source, attract and retain diverse and talented people, and create a sustainable, high-performing workforce.

We believe our staff is vital to the principle of making a positive difference to healthcare, therefore, we promote a culture of continuous personal development where scientists and staff have the support and resources to acquire new skills and build their careers through learning and development opportunities, coaching and clear career pathways.

We reserve the right to close any adverts once we have received a sufficient number of applications. If you decide to apply for this post but do not hear back from us within two weeks of your application, please assume that you have not been short-listed on this occasion.

SYNLAB UK & Ireland is a committed equal opportunities employer and does not unlawfully discriminate on the basis of any status or condition protected by applicable UK employment law.

Job description

Job responsibilities

Participate in and assist with clinical trials, the development of new tests and research & validation of equipment ensuring at all times compliance with all policies as required by regulatory directives, accreditation bodies and local management policies and practices.

To provide technical advice to clinical staff

To perform and interpret routine and specialist Biomedical investigations and to participate daily in the scientific and technical activities of the laboratory section under the supervision of senior staff.

Together with Senior staff help ensure compliance with all policies as required by regulatory directives, accreditation bodies and local management, including;

- United Kingdom Accreditation Services (UKAS) / Clinical Pathology Accreditation (CPA)

- Christie Pathology Partnership policies and SOPs

- MHRA

- NHSCSP

- HTA

- HFEA

Any other body in area of responsibility

Utilise the laboratory LIMS, Q-Pulse quality monitoring system and other application software according to authorised protocols including assisting in computer data entry in all areas of the laboratory, document review, non conformance review and quality assurance processes.

Communicate efficiently, courteously and with clarity at all times, whether face to face, telephone or electronic methods referring enquiries to senior staff where appropriate. Matters being communicated may include complex information and/or results.

Attend and participate positively in laboratory and other meetings as directed by Laboratory senior staff

As directed by senior laboratory staff, plan and prioritise work allocations, training plans, audits of both yourself and junior staff, responding appropriately to the needs of routine and urgent activities.

Encourage active participation in continuous professional development and support the introduction of new technologies and / or systems by being a change advocate.

Report all incidents and adverse events to senior staff and enter the information into Datix in a timely manner.

Demonstrate on going competency against training plans and participate positively in CPD (continuous professional development) activities.

Safety:

To observe safety regulations and attend mandatory fire, manual handling and other course as required.

To assist in the investigations of any incidents.

Participate in risk assessment monitoring

To ensure that the equipment within area of work is maintained and operated as per SOPs

To comply with The Christie policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies

Person Specification

Experience

Essential

  • At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training

Qualifications

Essential

  • HCPC State Registration as a Biomedical Scientist in Blood Sciences discipline
  • BSc (Hons) Biomedical degree or equivalent
  • IBMS Specialist Portfolio or equivalent

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.

UK Registration

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

Employer details

Employer name

The Christie Pathology Partnership LLP

Address

550 Wilmslow Road

Withington

Manchester

M20 4BX


Job Ad Reference E0336-24-0004
Date Listed 14 June 2024
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