About the role
About the job: The purpose of the post is to provide clinical diagnostic expertise for the Genomics section of the Precision Medicine Centre of Excellence.
For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.
The post holder is expected to assist the clinical genomics area of the laboratory in the development, validation and reporting of molecular pathology investigations, including the design and implementation of clinical genomics protocols for precision cancer medicine in haematological and solid tumours.
To assist with day-to-day planning and coordination of reporting activities, quality management and training.
Analysing and interpreting large amounts of biological, clinical and scientific data, including genomics and transcriptomics providing timely and accurate feedback in close collaboration with the Genomics Lead and bioinformatics team.
The successful candidate will be expected to integrate into a multidisciplinary environment, and to interact with key clinical and scientific stakeholders.
We will consider requests for part-time working to a minimum of 0.6fte.
About the person: The successful candidate must have, and your application should clearly demonstrate that you meet the following essential criteria: Have obtained a higher degree (PhD or MSc) in cancer genomics, molecular pathology, applied genomics, human genetics, or related discipline.
Hold current HCPC registration as a Clinical Scientist with current scope of activity in Molecular Pathology of Acquired Disease, or equivalent international qualification.
Minimum 5 years relevant, significant and demonstrable post-registration clinical experience in Molecular Pathology of Acquired Disease (solid tumors and/or molecular haemato-oncology). xwzovoh
Significant and demonstrable experience in validating, implementing, analysing and reporting a wide range of routine diagnostic/clinical molecular pathology tests using various genomic methods and sample types (including FFPE, HMW DNA, ctDNA testing) Significant and demonstrable experience in designing, developing, managing and analysing NGS technologies and data Significant and demonstrable experience in reporting high volumes of molecular pathology NGS tests in solid tumors and/or molecular haemato-oncology, including participation in EQA To be successful at shortlisting stage, please ensure you clearly evidence in your application how you meet the essential and, where applicable, desirable criteria listed in the Candidate Information document on our website.
TPBN1_NI
For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.
The post holder is expected to assist the clinical genomics area of the laboratory in the development, validation and reporting of molecular pathology investigations, including the design and implementation of clinical genomics protocols for precision cancer medicine in haematological and solid tumours.
To assist with day-to-day planning and coordination of reporting activities, quality management and training.
Analysing and interpreting large amounts of biological, clinical and scientific data, including genomics and transcriptomics providing timely and accurate feedback in close collaboration with the Genomics Lead and bioinformatics team.
The successful candidate will be expected to integrate into a multidisciplinary environment, and to interact with key clinical and scientific stakeholders.
We will consider requests for part-time working to a minimum of 0.6fte.
About the person: The successful candidate must have, and your application should clearly demonstrate that you meet the following essential criteria: Have obtained a higher degree (PhD or MSc) in cancer genomics, molecular pathology, applied genomics, human genetics, or related discipline.
Hold current HCPC registration as a Clinical Scientist with current scope of activity in Molecular Pathology of Acquired Disease, or equivalent international qualification.
Minimum 5 years relevant, significant and demonstrable post-registration clinical experience in Molecular Pathology of Acquired Disease (solid tumors and/or molecular haemato-oncology). xwzovoh
Significant and demonstrable experience in validating, implementing, analysing and reporting a wide range of routine diagnostic/clinical molecular pathology tests using various genomic methods and sample types (including FFPE, HMW DNA, ctDNA testing) Significant and demonstrable experience in designing, developing, managing and analysing NGS technologies and data Significant and demonstrable experience in reporting high volumes of molecular pathology NGS tests in solid tumors and/or molecular haemato-oncology, including participation in EQA To be successful at shortlisting stage, please ensure you clearly evidence in your application how you meet the essential and, where applicable, desirable criteria listed in the Candidate Information document on our website.
TPBN1_NI
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