People are the foundation of the CCTU's success. Build a career in a unit that supports life-changing clinical research.
We improve people's quality of life by supporting innovative and sustainable healthcare research to support safe, kind and excellent delivery of healthcare. We foster an inclusive culture that promotes equality of opportunity, values diversity and maintains a working environment in which the rights and dignity of all our staff are respected. Personal and professional development is key to enabling individuals to reach their full potential and maximise their contribution to the CCTU.
Applications are invited for the following post(s):
Clinical Trials Monitor
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Main area: Clinical Trials |
Employer: Cambridge University Hospitals NHS Foundation Trust |
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Grade: Band 6 |
Employer Type: NHS |
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Contract: 24 months (Fixed Term for 24 months) |
Site: Addenbrookes Hospital - R&D |
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Hours: Full time - 37.5 hours per week (requires some office based working) |
Town: Cambridge |
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Job ref: 180-RD-245192 |
Salary: £35,392 - £42,618 |
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Closing: 27-May-2024 23:59 |
Salary period: Yearly |
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Interview date: 12-Jun-2024 |
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Job overview: The Monitor will have responsibility for the essential monitoring of non-commercial clinical trials sponsored by Cambridge University Hospitals NHS Foundation Trust to ensure compliance in accordance with Good Clinical Practice (GCP) Guidelines, the Research Governance Framework for Health & Social Care (2005) and the Medicines for human Use (Clinical Trials) Regulations 2004. The post holder will work with colleagues in the Cambridge Clinical Trials Unit (CCTU) to support monitoring provision of Trust Sponsored Clinical Trials, and support for clinical researchers, under the guidance of a Senior Clinical Trial Monitor. Main duties: To review the Clinical Trial Risk Assessment and contribute to updates throughout the duration of the trial. To develop a clinical trials monitoring plan based upon the Clinical Trial Risk Assessment and an understanding of the key trial documentation. To be responsible for monitoring the conduct, documentation and progress of each clinical trial by performing risk based monitoring in accordance with the trial Monitoring Plan. To complete written monitoring visit reports on the progress, management and conduct of clinical trial undertaken at the Trust. To analyse any potential problems and make recommendations to rectify these under the guidance of the Senior Clinical Trial Monitor. |
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For more information and to apply online now |
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Clinical Trials Coordinator
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Main area: R&D - Clinical Trials Unite Cancer Theme |
Employer: Cambridge University Hospitals NHS Foundation Trust |
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Grade: Band 6 |
Employer Type: NHS |
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Contract: 12 months (Fixed Term for 12 months) |
Site: Addenbrookes Hospital-Division B |
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Hours: Full time - 37.5 hours per week (requires some office based working) |
Town: Cambridge |
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Job ref: 180-RD-245195 |
Salary: £35,392 - £42,618 |
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Closing: 15/05/2024 23:59 |
Salary period: Yearly |
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Interview date: 28/05/2024 |
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Job overview: We are looking for a Clinical Trial Coordinator to be part of the well-established Cancer Theme of the Cambridge Clinical Trials Unit. This is a non-patient facing position, requiring a candidate with clinical trials and/or project management experience. You will have primary responsibility for coordinating a multicentre clinical trial of an investigational medicinal product (CTIMP) in the urological malignancies field. Your day to day job will involve working closely with data managers, laboratory staff, statisticians and programmers, but also to liaise with medical staff involved in oncology trials and monitor the conduct of the studies. You will interact with regulatory authorities and collaborators, produce reports to stakeholders, and work in accordance with nationally agreed standards. This post is funded for 1 year, in the first instance, with the potential for contract renewal, dependent upon funding. The job is a hybrid role, involving mandatory office presence in Cambridge of at least 1 day a week. Main duties: Coordinate the setup and conduct of clinical trials and/or clinical studies working closely with the chief investigators and their teams. Setup participating sites in multi-centre trials and ensuring that all data and samples are collected following the protocol. To work in compliance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP), the NHS Research Governance Framework for Health & Social Care and, in the case of a CTIMP, in compliance with the Medicines for Human Use (Clinical Trials) Regulations 2004. |
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For more information and to apply online now |
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