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About the role
An opportunity has become available to join a clinical team undertaking Phase I clinical evaluation of novel CAR-T cell therapeutics in children with malignant brain tumours, which will be conducted at Great Ormond Street Hospital in partnership with the UCL Institute of Child Health. The post holder will be a clinician with significant experience in the management of children with cancer and will have an academic and clinical interest in the evaluation of experimental therapeutics within clinical trials. The appointee will have responsibility for recruitment to and management of patients and clinical data collection from the trial as well as supporting the patient management and data collection in other phase I studies. The appointee will fall under the overall line management of Professors Darren Hargrave (clinical PI) and John Anderson (scientific CI). This salary offered on this post is £65,048 – £73,992 per annum, nodal point 4-5 on the resident doctor pay scale and is funded until 28/02/2028 in the first instance.
About you
Main purpose summarised as follows:
• Responsible for day to day running of phase I clinical trial of CARTUNE clinical trial in paediatric brain tumour patients.
• Clinical data collection and quality analysis of CARTUNE trial patients.
• Liaison with manufacturing and laboratory teams for organization of trial related procedure
• Working with sponsor and manufacturing teams to coordinate regulatory submissions for parallel trials The ideal candidate for this post will be a medical doctor with specialist training in paediatrics and paediatric oncology, and interest in academic clinical trials and translational medicine. Applications from candidates interested in registering for research degrees are particularly welcome Duties and responsibilities:
• To be responsible for the organisation and co-ordination of patients enrolled on CARTUNE clinical trial.
• To contribute to the management of trial patients on related phase I studies at Great Ormond Street Hospital.
• To problem solve logistical issues related to day to day management of patients undergoing complex investigation cell therapies
• To ensure that the trial operates in accordance with current policies, relevant regulatory requirements and with due regard to underpinning scientific and ethical principles. To ensure compliance with University, Hospital, HTA regulations
• To link with the preclinical team and development and regulatory submissions for other experimental therapeutics cell therapy paediatric trials.
• To participate in teaching and training of junior or new members of the trials team
• To coordinate the opening of CARTUNE and other cell therapy trials at satellite clinical sites.
• To contribute to the drafting and submission of meeting abstracts, posters and research manuscripts
Customer advert reference: B02-10586