Full Time Biomedical jobs in London
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- Guy's and St Thomas' NHS Foundation TrustLondon SE1
- 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.
- Guy's and St Thomas' NHS Foundation TrustLondon SE1
- The Assisted Conception Unit at Guy’s and St Thomas’ Hospital is seeking a full-time Laboratory Manager to oversee the day to day running of the laboratory and…
- NovartisLondon
- Responsible for implementing high-quality, data strategy planning within clinical programs, supporting downstream clinical assessment identification and…
- View all Novartis jobs - London jobs - Clinical Data Manager jobs in London
- Salary Search: Clinical Data Strategy, Manager salaries in London
- See popular questions & answers about Novartis
- NovartisLondon
- Responsible for implementing high-quality, data strategy planning within clinical programs, supporting downstream clinical assessment identification and…
- View all Novartis jobs - London jobs - Clinical Data Manager jobs in London
- Salary Search: Clinical Data Strategy, Manager salaries in London
- See popular questions & answers about Novartis
- Nucs AILondon
- PhD in machine learning, computer vision, medical image analysis, biomedical engineering, or related field.
- We’re venture-backed, early-stage, and building a…
- View all Nucs AI jobs - London jobs - Machine Learning Engineer jobs in London
- Salary Search: Machine Learning Scientist salaries in London
Quality Technician (pharmaceutical)
Often replies in 3 daysAspire LaboratoriesDagenham- Company pension
- Casual dress
- On-site parking
- This is a full time, 5 days on site position.*.
- Job Types: Full-time, Permanent.
- Job Types: Full-time, Permanent.
- Ensure laboratory compliance with GMP.
- Medpace, Inc.London EC4V 3BJ
- Annual leave
- Company events
- Medpace is a full-service clinical contract research organization (CRO).
- Bachelor’s, or Master’s degree in informatics, computer science/engineering, biomedical…
- View all Medpace, Inc. jobs - London jobs - Analyst jobs in London
- Salary Search: Feasibility Informatics Analyst salaries in London
- See popular questions & answers about Medpace, Inc.
- Drive success of early global programs, develop and implement strategies to achieve Transition Decision Point (TDP).
- Fluent oral and written English.
- NovartisLondon
- Accountable for development and implementation of the biomarker strategy for a portfolio of program(s)/disease indication and coordinates biomarker and…
- View all Novartis jobs - London jobs - Regional Director jobs in London
- Salary Search: Director, Therapeutic Area Biomarker Lead (Neuroscience) salaries in London
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View similar jobs with this employerLifeArcLondon WC1H- Annual leave
- Company pension
- Private medical insurance
- Extensive experience in biomedical, life sciences, or translational and clinical research environments, including experience of driving and influencing…
- View all LifeArc jobs - London jobs - Director jobs in London
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- Boehringer Ingelheim Ltd.London
- It could be electronic health records and medical imaging to support patient segmentation.
- It could be ‘omics data to identify novel therapeutic targets.
- CoMindLondon
- Employee discount
- Unlimited paid holidays
- Private dental insurance
- Company pension
- PhD in biomedical optics, medical physics, biomedical engineering, optical engineering, or a related discipline.
- This is a hands-on senior scientific role.
- View all CoMind jobs - London jobs - Senior Research Scientist jobs in London
- Salary Search: Senior Optical Research Scientist salaries in London
- ICRSutton SM2 5NG
- Duration of Contract: For Career Faculty Non time limited.
- For Career Development Faculty appointments are made at £66,092 in the first instance.
- View all ICR jobs - Sutton jobs - Group Leader jobs in Sutton
- Salary Search: Group Leader - Cancer Health Data Sciences salaries in Sutton
- See popular questions & answers about ICR
- IXICOLondon
- Referral programme
- Annual leave
- Employee discount
- Employee assistance programme
- Company pension
- Private medical insurance
- To help us deliver our medical image analysis solutions to large clinical trials we are hiring a Senior Research Engineer on a permanent full-time capacity.
- View all IXICO jobs - London jobs
- Salary Search: Senior Research Engineer salaries in London
- North West London PathologyLondon W6 8RF
- Company pension
- Cycle to work scheme
- Car scheme
- Season ticket loan
- Participate in surgical dissection of diagnostic histopathology specimens with a particular focus on category D-E.
- IPP Analytics LimitedBasildon SS14 3BY
- Performing and interpreting routine and specialist biomedical investigations.
- Offering technical advice to clinicians regarding appropriate tests and turnaround…
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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