321 Oncology jobs in the United Kingdom
Clinical Oncology Consultant
Derby, East Midlands
£60000 - £90000 annum
Hope Homecare Services Limited
Posted 134 days ago
Job Viewed
Job Description
Contact
Experience Required: NHS experience essential
We are seeking an experienced and dedicated Clinical Oncology Consultant to join a leading healthcare provider in Derby . This permanent role offers an excellent opportunity to contribute to a dynamic oncology team, providing high-quality cancer care within an NHS setting.
Key Responsibilities:- Provide specialist clinical oncology services, including chemotherapy and radiotherapy treatment planning.
- Lead and support multidisciplinary team meetings, collaborating with oncologists, radiologists, surgeons, and other healthcare professionals.
- Develop and implement patient treatment plans, ensuring the highest standards of care and patient safety.
- Supervise and train junior doctors, nurses, and other healthcare staff.
- Participate in research, audits, and quality improvement initiatives within the department.
- Maintain up-to-date knowledge of advancements in oncology treatments and best practices.
- Engage in teaching activities for medical students and junior staff.
- Contribute to service development and clinical governance within the department.
Requirements
Full GMC registration with a license to practice.
CCT (Certificate of Completion of Training) in Clinical Oncology or eligibility within six months.
Extensive NHS experience in oncology.
Strong leadership, communication, and team-working skills.
Experience in chemotherapy, radiotherapy planning, and multidisciplinary team collaboration.
Benefits
- Competitive salary and NHS benefits package.
- Opportunities for professional development and research.
- Supportive and well-established oncology department.
- Access to state-of-the-art treatment facilities and cutting-edge technology.
If you are an experienced Clinical Oncology Consultant looking for a new opportunity in Derby , we would love to hear from you.
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Clinical Research Associate - Oncology
NR1 1AA Norwich, Eastern
£40000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
WhatJobs is seeking a dedicated and experienced Clinical Research Associate (CRA) to join a growing pharmaceutical company with operations in Norwich, Norfolk, UK . This hybrid role involves managing and monitoring clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as data verification and ensuring patient safety. The ideal candidate will have a strong background in clinical research, excellent attention to detail, and a passion for advancing oncology treatments. This is a crucial role in bringing life-changing therapies to patients.
Responsibilities:
Qualifications:
This is an exciting opportunity to contribute to critical oncology research and development.
Responsibilities:
- Conduct pre-study, initiation, interim, and close-out site visits according to protocol and regulatory requirements.
- Assess the suitability of potential sites and investigators for clinical trials.
- Train and support site staff on study procedures, protocols, and regulatory compliance.
- Monitor study conduct to ensure adherence to the protocol, GCP, and applicable regulations.
- Verify the accuracy and completeness of clinical data collected at study sites.
- Manage study documentation and ensure essential documents are maintained in site files.
- Report adverse events and serious adverse events promptly according to company and regulatory guidelines.
- Build and maintain strong working relationships with investigators, site staff, and internal project teams.
- Prepare and present site monitoring reports and action plans.
- Ensure timely resolution of site-related issues and implement corrective actions.
- Contribute to the development of study protocols and clinical study reports.
- Participate in investigator meetings and training sessions.
- Maintain up-to-date knowledge of oncology therapies and clinical research trends.
- Communicate effectively with internal stakeholders, including project managers, medical monitors, and data managers.
- Ensure data integrity and patient safety throughout the clinical trial process.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate, preferably with oncology experience.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in conducting site monitoring visits and managing study sites.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical, problem-solving, and decision-making skills.
- Exceptional communication, interpersonal, and organizational skills.
- Ability to work independently and manage travel effectively for site visits.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Familiarity with the pharmaceutical and clinical research landscape in Norwich, Norfolk, UK is a plus.
- Commitment to patient safety and data integrity.
This is an exciting opportunity to contribute to critical oncology research and development.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Scientist - Oncology
NE1 4XX Newcastle upon Tyne, North East
£65000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading global pharmaceutical company at the forefront of developing life-saving therapies, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their esteemed research team. This vital role involves contributing significantly to the design, execution, and interpretation of clinical trials for novel cancer treatments. You will be responsible for developing clinical trial protocols, collaborating with investigators and study sites, and ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. A deep understanding of oncology drug development, disease mechanisms, and clinical trial methodologies is crucial. You will analyze study data, contribute to the preparation of regulatory submissions, and present findings at scientific conferences. The ideal candidate will possess excellent scientific acumen, strong analytical skills, and the ability to work effectively within multidisciplinary teams. Experience in oncology clinical research, including phases I-IV, is highly preferred. This position requires meticulous attention to detail, strong problem-solving abilities, and a commitment to advancing cancer care. You will play a key role in bringing innovative treatments to patients who need them most. Collaboration with internal stakeholders, including medical affairs, regulatory affairs, and commercial teams, will be a significant part of your responsibilities. A Ph.D. or MD in a relevant scientific or medical discipline, along with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, is required. Excellent written and verbal communication skills in English are essential. This is an on-site position located at our client's state-of-the-art facilities in Newcastle upon Tyne, Tyne and Wear, UK , offering a dynamic and collaborative research environment.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Director - Oncology
BD1 1AA Bradford, Yorkshire and the Humber
£90000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer therapies, is seeking a highly accomplished Clinical Research Director to lead critical oncology studies. This pivotal role is based in our state-of-the-art facility in Bradford, West Yorkshire, UK , and involves overseeing the design, execution, and completion of complex clinical trials. The successful candidate will be responsible for ensuring that all research is conducted in compliance with regulatory standards, ethical guidelines, and company objectives. You will manage a team of clinical research professionals, foster collaborations with key opinion leaders, and contribute to the development of life-saving medications.
Responsibilities:
Responsibilities:
- Direct the strategic planning and operational execution of oncology clinical development programs.
- Oversee the design and protocol development for Phase I-IV clinical trials, ensuring scientific rigor and regulatory compliance.
- Manage study budgets, timelines, and resources effectively to ensure timely and successful trial completion.
- Lead and mentor a high-performing team of clinical scientists, study managers, and monitors.
- Ensure adherence to Good Clinical Practice (GCP), FDA, EMA, and other relevant regulatory guidelines.
- Collaborate with internal departments (e.g., R&D, Regulatory Affairs, Biostatistics) and external partners (e.g., investigators, CROs) to facilitate trial execution.
- Review and interpret clinical data, working closely with biostatisticians and medical writers.
- Contribute to regulatory submissions and interactions with health authorities.
- Stay abreast of the latest advancements in oncology research, treatment modalities, and clinical trial methodologies.
- Represent the company at scientific conferences and meetings.
- M.D., Ph.D., Pharm.D., or relevant advanced scientific degree.
- Minimum of 10 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a significant focus on oncology.
- Proven experience in leading and managing multiple complex clinical trials simultaneously.
- In-depth knowledge of clinical trial design, regulatory requirements (FDA, EMA, GCP), and drug development process.
- Strong leadership, team management, and cross-functional collaboration skills.
- Excellent scientific judgment, analytical skills, and problem-solving abilities.
- Outstanding written and verbal communication skills, with experience presenting complex scientific information.
- Experience working within or managing CRO relationships.
- This is a primarily office-based role requiring regular attendance at our Bradford, West Yorkshire, UK location to facilitate team collaboration and facility access. Limited travel may be required for specific project needs or conferences.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Scientist - Oncology
LS1 1UR Leeds, Yorkshire and the Humber
£60000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to advancing cancer therapies, is seeking an accomplished Clinical Research Scientist to join their innovative oncology division. This hybrid role, based at their state-of-the-art facility in Leeds, West Yorkshire, UK , offers the opportunity to contribute to life-saving drug development while maintaining a flexible work-life balance.
You will be instrumental in the design, execution, and analysis of clinical trials, focusing on the development of novel oncology treatments. This role requires a strong scientific background, a deep understanding of clinical trial methodologies, and the ability to interpret complex scientific data. You will collaborate with cross-functional teams, including medical affairs, regulatory, and data management, to ensure the successful progression of research programmes.
Key Responsibilities:
Qualifications:
This is a challenging and rewarding position offering the chance to make a tangible impact on the lives of patients. Join a world-class team at the forefront of cancer research in Leeds, West Yorkshire, UK .
You will be instrumental in the design, execution, and analysis of clinical trials, focusing on the development of novel oncology treatments. This role requires a strong scientific background, a deep understanding of clinical trial methodologies, and the ability to interpret complex scientific data. You will collaborate with cross-functional teams, including medical affairs, regulatory, and data management, to ensure the successful progression of research programmes.
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with regulatory guidelines and company objectives.
- Oversee the operational aspects of clinical trials, ensuring adherence to Good Clinical Practice (GCP).
- Monitor study progress, analyse data, and interpret results to guide decision-making.
- Collaborate with investigators, clinical research associates (CRAs), and study teams to ensure trial integrity.
- Prepare and present scientific findings at internal meetings and external conferences.
- Contribute to the preparation of regulatory submissions and scientific publications.
- Identify and evaluate potential new drug candidates and therapeutic strategies.
- Ensure compliance with all relevant safety regulations and ethical standards.
- Stay abreast of the latest scientific advancements and industry trends in oncology research.
- Mentor junior members of the research team.
Qualifications:
- PhD or equivalent in a relevant life science discipline (e.g., Oncology, Pharmacology, Molecular Biology, Immunology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry, with a focus on oncology.
- Proven experience in clinical trial design, protocol development, and execution.
- Strong understanding of GCP, regulatory requirements (e.g., FDA, EMA), and drug development processes.
- Excellent analytical and problem-solving skills, with the ability to critically evaluate scientific data.
- Proficiency in scientific literature review and data interpretation.
- Strong written and verbal communication skills, with experience in scientific writing.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Experience with data analysis software and statistical interpretation is desirable.
This is a challenging and rewarding position offering the chance to make a tangible impact on the lives of patients. Join a world-class team at the forefront of cancer research in Leeds, West Yorkshire, UK .
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Scientist - Oncology
SO15 0AA Southampton, South East
£50000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
A leading pharmaceutical company is looking for a dedicated and highly skilled Clinical Research Scientist specializing in Oncology to be based at their state-of-the-art facility in Southampton, Hampshire, UK . This crucial role will involve contributing to the design, execution, and analysis of clinical trials for novel cancer therapies. You will work within a multidisciplinary team of scientists, clinicians, and statisticians, playing a key part in advancing our understanding and treatment of various oncological conditions. The responsibilities include protocol development, study site selection, investigator training, monitoring trial progress, data interpretation, and contributing to regulatory submissions. The ideal candidate will have a strong background in oncology research, extensive knowledge of clinical trial methodologies, and a thorough understanding of relevant regulatory guidelines (e.g., GCP, FDA, EMA). You should possess excellent analytical and problem-solving skills, with the ability to critically evaluate complex scientific data. Experience with statistical analysis software and data management systems is highly desirable. This position requires meticulous attention to detail, strong organizational abilities, and the capacity to manage multiple projects effectively. You will be expected to author scientific reports, present findings at conferences, and contribute to publications in peer-reviewed journals. The ability to communicate complex scientific information clearly and concisely to both expert and non-expert audiences is essential. This is an exciting opportunity to contribute to life-saving medical advancements in a collaborative and dynamic research environment. Join our team in Southampton and help drive innovation in cancer treatment.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Scientist - Oncology
CF10 1AA Cardiff, Wales
£55000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Clinical Research Scientist to join their dynamic team in Cardiff, Wales, UK . This hybrid role requires a strong scientific background and a passion for advancing cancer treatments. You will play a crucial role in the design, execution, and analysis of clinical trials, contributing directly to the development of life-saving therapies. The successful candidate will collaborate with cross-functional teams, including clinicians, statisticians, and regulatory affairs specialists, to ensure the highest standards of scientific integrity and patient safety.
Responsibilities:
Qualifications:
This is an exceptional opportunity to contribute to groundbreaking research in oncology and make a tangible difference in patients' lives. Join our client's dedicated team and help drive the future of cancer treatment.
Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific validity and regulatory compliance.
- Oversee the operational aspects of clinical trials, including site selection, monitoring, and data collection.
- Analyze and interpret complex clinical data, identifying key trends and insights.
- Prepare scientific reports, publications, and presentations for internal and external stakeholders.
- Collaborate with PIs and study coordinators to ensure protocol adherence and patient safety.
- Manage relationships with contract research organizations (CROs) and other external partners.
- Stay current with scientific literature, emerging technologies, and regulatory guidelines in oncology.
- Contribute to the strategic planning and decision-making processes within the R&D department.
- Mentor junior research staff and contribute to a collaborative research environment.
- Ensure all research activities are conducted in accordance with Good Clinical Practice (GCP) guidelines.
Qualifications:
- Ph.D. or Pharm.D. in a relevant life science discipline (e.g., Pharmacology, Oncology, Immunology, Biomedical Science).
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a focus on oncology.
- Demonstrated experience in designing and managing Phase I-III clinical trials.
- Strong understanding of oncology drug development pathways and mechanisms of action.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in statistical analysis software (e.g., SAS, R) is a plus.
- Exceptional written and verbal communication skills.
- Ability to work effectively in a team-oriented, fast-paced environment.
- Experience with data management systems and electronic data capture (EDC) tools.
- Knowledge of international regulatory requirements (e.g., FDA, EMA).
This is an exceptional opportunity to contribute to groundbreaking research in oncology and make a tangible difference in patients' lives. Join our client's dedicated team and help drive the future of cancer treatment.
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6
Clinical Research Scientist - Oncology
NE1 7RU Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated Clinical Research Scientist with a specialization in Oncology. This hybrid role, based in **Newcastle upon Tyne, Tyne and Wear, UK**, offers a unique opportunity to contribute to groundbreaking research aimed at improving cancer treatment outcomes. You will be involved in the design, execution, and analysis of clinical trials, working collaboratively with cross-functional teams. The ideal candidate will possess a strong scientific background, excellent analytical skills, and a passion for advancing medical knowledge. This position requires a balance of on-site laboratory and office work, complemented by remote flexibility for data analysis and report writing.
Key Responsibilities:
Qualifications:
This is an exciting role for a scientifically driven individual looking to make a real impact in cancer research. You will be part of a collaborative environment that fosters innovation and professional growth. The **location** is **Newcastle upon Tyne, Tyne and Wear, UK**, with a hybrid working arrangement. If you are passionate about clinical research and have a strong background in oncology, we encourage you to apply.
Key Responsibilities:
- Contribute to the design and development of clinical trial protocols in oncology.
- Oversee the execution of clinical trials, ensuring adherence to scientific rigor and regulatory requirements.
- Collect, manage, and analyse complex biological and clinical data.
- Interpret study results and contribute to the preparation of scientific reports and publications.
- Collaborate with internal teams (e.g., medical affairs, regulatory, R&D) and external investigators.
- Stay current with scientific literature and advancements in oncology and clinical research.
- Contribute to the identification of new therapeutic targets and strategies.
- Prepare presentations for scientific meetings and conferences.
- Ensure compliance with Good Clinical Practice (GCP) guidelines.
- Assist in the preparation of regulatory submissions.
Qualifications:
- PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 3 years of experience in clinical research, preferably within the pharmaceutical or biotech industry.
- Demonstrated expertise in oncology research.
- Strong understanding of clinical trial design, methodology, and regulatory landscape.
- Proficiency in data analysis and statistical software.
- Excellent scientific writing and communication skills.
- Ability to work effectively in a multidisciplinary team.
- Strong analytical and problem-solving abilities.
- Experience with hybrid work models, balancing on-site and remote responsibilities.
- Knowledge of drug development processes.
This is an exciting role for a scientifically driven individual looking to make a real impact in cancer research. You will be part of a collaborative environment that fosters innovation and professional growth. The **location** is **Newcastle upon Tyne, Tyne and Wear, UK**, with a hybrid working arrangement. If you are passionate about clinical research and have a strong background in oncology, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Scientist - Oncology
OX1 3PA Oxford, South East
£55000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their esteemed research and development team in Oxford, Oxfordshire, UK . This role is crucial for advancing groundbreaking cancer therapies from preclinical stages through to clinical trials. The successful candidate will be responsible for designing, executing, and interpreting complex experiments, analyzing data, and contributing to the strategic direction of oncology drug development programs. You will work at the forefront of medical science, collaborating with a multidisciplinary team of scientists, clinicians, and project managers. This is a hybrid role, requiring a balance of in-lab research and remote data analysis and reporting, fostering a dynamic and flexible working environment.
Key Responsibilities:
Qualifications and Experience:
Key Responsibilities:
- Design and conduct in vitro and in vivo studies to evaluate novel oncology drug candidates.
- Develop and validate experimental assays and methodologies relevant to cancer biology.
- Analyze and interpret complex biological and pharmacological data, generating high-quality reports.
- Contribute to the preparation of regulatory submissions (e.g., IND, CTA) and scientific publications.
- Stay abreast of the latest scientific literature and technological advancements in oncology and drug discovery.
- Collaborate effectively with internal teams (e.g., discovery biology, toxicology, clinical development) and external partners.
- Present research findings at internal meetings and external scientific conferences.
- Contribute to the selection of lead candidates for clinical development.
- Ensure all research activities comply with ethical guidelines, regulatory requirements, and company SOPs.
- Mentor junior scientists and contribute to a culture of scientific excellence and innovation.
Qualifications and Experience:
- Ph.D. in Cancer Biology, Pharmacology, Molecular Biology, or a related field.
- Proven track record of research in oncology drug discovery and development.
- Extensive hands-on experience with relevant experimental techniques (e.g., cell culture, molecular biology assays, in vivo models).
- Strong data analysis skills and experience with statistical software.
- Excellent written and oral communication skills, with a proven ability to publish and present scientific work.
- Demonstrated ability to work independently and collaboratively in a hybrid team setting.
- Knowledge of regulatory pathways for drug approval is a plus.
- Experience with bioinformatics tools and techniques is advantageous.
- Strong problem-solving abilities and a creative approach to scientific challenges.
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8
Clinical Research Scientist - Oncology
SW1A 0AA London, London
£70000 Annually
WhatJobs
Posted 16 days ago
Job Viewed
Job Description
Our client , a leading biopharmaceutical company, is seeking a highly skilled and motivated Clinical Research Scientist to join their dynamic oncology research team in London . This hybrid role offers the opportunity to contribute to groundbreaking research aimed at developing novel therapies for cancer patients. You will be instrumental in designing, implementing, and overseeing clinical trials, working collaboratively with cross-functional teams.
As a Clinical Research Scientist, you will be responsible for the scientific integrity and execution of clinical studies. This involves protocol development, site selection, data analysis, and interpretation of results. You will play a key role in ensuring that trials are conducted in compliance with regulatory requirements, ethical standards, and company policies. Your expertise will be vital in advancing our understanding of cancer biology and translating scientific discoveries into clinical applications.
Key responsibilities include:
The ideal candidate will hold a Ph.D. or M.D. in a relevant life science or medical field, with a strong track record in oncology clinical research. A minimum of 5 years of experience in the pharmaceutical or biotechnology industry, managing clinical trials, is required. Comprehensive knowledge of cancer biology, clinical trial design, and regulatory landscapes is essential. Excellent analytical, communication, and leadership skills are necessary to effectively manage complex projects and collaborate with diverse teams. This is an exciting opportunity to contribute to innovative cancer research in London and make a significant impact on patient outcomes.
As a Clinical Research Scientist, you will be responsible for the scientific integrity and execution of clinical studies. This involves protocol development, site selection, data analysis, and interpretation of results. You will play a key role in ensuring that trials are conducted in compliance with regulatory requirements, ethical standards, and company policies. Your expertise will be vital in advancing our understanding of cancer biology and translating scientific discoveries into clinical applications.
Key responsibilities include:
- Developing and refining clinical trial protocols for oncology studies, ensuring scientific validity and feasibility.
- Selecting and managing clinical trial sites, including investigator meetings and site initiation visits.
- Overseeing data collection and monitoring the quality of data generated from clinical trials.
- Performing statistical analysis and interpreting clinical trial data in collaboration with biostatisticians.
- Preparing clinical study reports, manuscripts for publication, and regulatory submission documents.
- Ensuring adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
- Collaborating with internal teams, including medical affairs, regulatory affairs, and drug development.
- Presenting research findings at scientific conferences and internal meetings.
- Providing scientific expertise and guidance to clinical development teams.
The ideal candidate will hold a Ph.D. or M.D. in a relevant life science or medical field, with a strong track record in oncology clinical research. A minimum of 5 years of experience in the pharmaceutical or biotechnology industry, managing clinical trials, is required. Comprehensive knowledge of cancer biology, clinical trial design, and regulatory landscapes is essential. Excellent analytical, communication, and leadership skills are necessary to effectively manage complex projects and collaborate with diverse teams. This is an exciting opportunity to contribute to innovative cancer research in London and make a significant impact on patient outcomes.
This advertiser has chosen not to accept applicants from your region.
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