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- Guy's and St Thomas' NHS Foundation TrustLondon SE1
- After completing a fully comprehensive induction package you will find yourself leading the co-ordination of an agreed portfolio of clinical trials, assisting…
Associate Director Life Sciences
Often replies in 4 daysBuro HappoldLondon EC1Y 2AL- Employee discount
- Employee assistance programme
- Company pension
- Cycle to work scheme
- Responding to strong local and international drivers for purposeful and sustainable building design - in particular, working with other senior leaders across…
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- University of SurreyGuildford
- As a Lecturer/Senior Lecturer/Associate Professor, you will be expected to develop and lead a significant externally funded programme of research in line with…
- Cardiff Metropolitan UniversityCardiff
- You will be required to make a significant contribution to the delivery of our taught portfolio contributing to the delivery on the BSc Biomedical Science, BSc…
View similar jobs with this employerAvantorCambridge- Company pension
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View similar jobs with this employerAvantorCambridge- Company pension
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- Cerca Magnetics LimitedNottingham
- Excellent communication skills and confidence working with international customers.
- Domestic & international travel (30–40%) to customer sites.
- StantecCambridge
- Company pension
- Private medical insurance
- Discounted gym membership
- The role would suit a transport planner with a broad understanding of all elements of the profession, ideally with a focus on transport planning for development…
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- The University of ManchesterManchester M13 9PL
- Annual leave
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- Producing and disseminating research outputs of national and international standing.
- A track record of excellence in research in the broad field of audiology…
- AstraZenecaCambridge
- Master’s degree in AI/ML with experience applying these methods to clinical and/or biomedical data.
- 5+ years experience developing AI/ML for clinical,…
- BSIRemote
- Flexible schedule
- This may include electronic/electrical, electro-mechanical or biomedical engineering or medical physics.
- BSI is seeking experienced medical device professionals…
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- MEDIDATALondon
- Annual leave
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- MedtronicLondon
- Ability to work remotely and productively for an international company spanning multiple time zones across the US and Europe.
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- University of WolverhamptonWolverhampton
- Annual leave
- Employee discount
- Employee assistance programme
- Free parking
- Company pension
- Discounted gym membership
- You will have a developing track record in research in a relevant field, including research outputs that could contribute to the next REF exercise, and some…
- TUV Rheinland UK Ltd.Solihull B90 8BG
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- ICRSutton SM2 5NG
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Job Post Details
Clinical Research Practitioner - I - job post
3.63.6 out of 5 stars
London SE1
£38,488 - £46,852 a year - Full-time
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Job details
Pay
- £38,488 - £46,852 a year
Job type
- Full-time
Location
London SE1
Full job description
We are looking for candidates interested in building a career in research in one of the biggest oncology and haematology research teams in London. This Clinical Research Practitioner post will sit in our Lung Oncology Research Team.
After completing a fully comprehensive induction package you will find yourself leading the co-ordination of an agreed portfolio of clinical trials, assisting in trial set up, identifying patients and discussing trials with them, collecting and reporting data and supporting patients and their carers throughout treatment. Successful candidates will be excellent communicators with an eye for detail and a commitment to improving patient choices, care and outcomes.
If you have applied for this post in the last 3 months and have been unsuccessful, please do not apply
Acting as patient and participant advocate at all times, the post holder will be expected to co-ordinate research clinics and organise study related care. They will implement and evaluate strategies to identify and assist in the enrolment of research participants. The post-holder will lead on a portfolio of research studies and perform a range of clinical assessments in line with accepted standards of practice. They will communicate proactively with the study and clinical teams to ensure good participant experience and adherence to study protocols. The post holder will be responsible for case report form completion, site file management, implementation of amendments and maintenance of databases. They will act as mentor and support for new and junior team members. They will contribute to quality assurance processes within the team. The post holder will ensure the well-being of participants by adhering to study protocols, relevant regulations and local Standard Operating Procedures (SOPs).
We have a long tradition of clinical and scientific achievement and – as part of King’s Health Partners – we are one of England’s eight academic health sciences centres, bringing together world-class clinical services, teaching and research. We have one of the National Institute for Health Research’s biomedical research centres, established with King’s College London in 2007, as well as dedicated clinical research facilities.
The Lung Oncology Research team is based at Guy's Hospital.
Please refer to the attached job description and person specification which outlines the full and detailed responsibilities of this role. More information can be gained from contacting us on the details below.
Provide excellent customer care skills to ensure patients and participants come first.
Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the clinical trial protocol is adhered to at all times.
After completing a fully comprehensive induction package you will find yourself leading the co-ordination of an agreed portfolio of clinical trials, assisting in trial set up, identifying patients and discussing trials with them, collecting and reporting data and supporting patients and their carers throughout treatment. Successful candidates will be excellent communicators with an eye for detail and a commitment to improving patient choices, care and outcomes.
If you have applied for this post in the last 3 months and have been unsuccessful, please do not apply
Acting as patient and participant advocate at all times, the post holder will be expected to co-ordinate research clinics and organise study related care. They will implement and evaluate strategies to identify and assist in the enrolment of research participants. The post-holder will lead on a portfolio of research studies and perform a range of clinical assessments in line with accepted standards of practice. They will communicate proactively with the study and clinical teams to ensure good participant experience and adherence to study protocols. The post holder will be responsible for case report form completion, site file management, implementation of amendments and maintenance of databases. They will act as mentor and support for new and junior team members. They will contribute to quality assurance processes within the team. The post holder will ensure the well-being of participants by adhering to study protocols, relevant regulations and local Standard Operating Procedures (SOPs).
We have a long tradition of clinical and scientific achievement and – as part of King’s Health Partners – we are one of England’s eight academic health sciences centres, bringing together world-class clinical services, teaching and research. We have one of the National Institute for Health Research’s biomedical research centres, established with King’s College London in 2007, as well as dedicated clinical research facilities.
The Lung Oncology Research team is based at Guy's Hospital.
Please refer to the attached job description and person specification which outlines the full and detailed responsibilities of this role. More information can be gained from contacting us on the details below.
Provide excellent customer care skills to ensure patients and participants come first.
Work within relevant regulations and ICH GCP (International Conference on Harmonisation and Good Clinical Practice) ensuring that the clinical trial protocol is adhered to at all times.
- Lead on a portfolio of trials and coordinate participation. This requires liaising with the clinical team to organise and ensure that trial specific investigations are undertaken according to the protocol, paying particular attention to accurate data collection and dissemination and version control of essential documentation.
- Devise, implement and evaluate strategies for recruiting participants into clinical studies and identify individuals potentially eligible for research studies. Gain permissions for research contacts.
- Organise and facilitate participant appointments and follow-up phone calls.
- Update participant study and medical records to accurately document study related activity and procedures.
- Ensure the confidentiality of verbal, written and computerised information.
- Complete case report forms in a precise and timely manner, ensuring that all the relevant clinical data in the participant’s medical notes and study file is transcribed accurately.
- Responsible for the maintenance of the Investigator Site Files.
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