Explore opportunities in cancer research, a field dedicated to understanding, preventing, and treating cancer. Professionals in this area work across various disciplines, including biology, genetics, and medicine, to advance scientific knowledge and develop innovative therapies. Cancer research jobs involve laboratory work, clinical trials, data analysis, and scientific writing, contributing to improved patient outcomes and public health.6,785 Cancer Research jobs in the United Kingdom
Clinical Research Scientist
NG1 1GG Nottingham, East Midlands
£55000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical company dedicated to advancing global health, is looking for a highly skilled and motivated Clinical Research Scientist to join their esteemed research and development team based in Nottingham, Nottinghamshire, UK . This critical role involves contributing to the design, execution, and analysis of clinical trials for novel therapeutic agents. You will be responsible for the scientific integrity of clinical studies, ensuring compliance with regulatory requirements and ethical standards. Key duties include developing clinical protocols, managing data collection and analysis, interpreting study results, and preparing scientific reports and publications. You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external stakeholders such as investigators, ethics committees, and contract research organizations (CROs). The ideal candidate will possess a Ph.D. or Master's degree in a relevant life science discipline (e.g., pharmacology, biology, medicine) with significant experience in clinical research within the pharmaceutical industry. A strong understanding of drug development processes, Good Clinical Practice (GCP) guidelines, and regulatory frameworks (e.g., FDA, EMA) is essential. Excellent scientific writing, communication, and interpersonal skills are required to effectively present complex data and engage with diverse audiences. This is an exciting opportunity to contribute to the development of life-changing medicines and advance your career in a dynamic and supportive environment. The role requires presence in our Nottingham facility to facilitate essential in-person collaboration and laboratory work.
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Clinical Research Scientist
CF10 1DA Cardiff, Wales
£60000 Annually
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Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company committed to improving global health, is seeking a dedicated and experienced Clinical Research Scientist to join their dynamic team in **Cardiff**, Wales. This role is integral to the design, execution, and interpretation of clinical trials for novel therapeutic agents. You will play a key part in bringing life-changing medicines to patients by ensuring the highest standards of scientific integrity and regulatory compliance throughout the clinical development process. The ideal candidate will possess a strong scientific background, extensive experience in clinical trial management, and a deep understanding of regulatory guidelines (e.g., ICH-GCP). Responsibilities include developing clinical trial protocols, overseeing study conduct, managing data analysis and interpretation, and preparing regulatory submissions. You will collaborate closely with internal teams, including R&D, regulatory affairs, and project management, as well as external partners such as investigators, site staff, and contract research organizations (CROs). This position requires exceptional analytical, problem-solving, and communication skills, as well as the ability to work effectively in a collaborative, fast-paced environment. This role is office-based in **Cardiff**. We offer a competitive salary, comprehensive benefits package, and opportunities for professional growth and development within a company that values innovation and scientific excellence.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with scientific objectives and regulatory requirements.
- Oversee the execution of clinical trials, ensuring compliance with ICH-GCP and other relevant regulations.
- Manage study timelines, budgets, and resources effectively.
- Collaborate with investigators and clinical site staff to ensure high-quality data collection.
- Analyze and interpret clinical trial data, contributing to study reports and publications.
- Prepare study-related documents, including investigator brochures, case report forms, and regulatory submission dossiers.
- Liaise with regulatory authorities and ethics committees.
- Contribute to the scientific strategy for drug development programs.
- Mentor and guide junior research staff.
Qualifications:
- PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research and development within the pharmaceutical industry.
- Thorough understanding of clinical trial design, execution, and data analysis.
- In-depth knowledge of ICH-GCP guidelines and regulatory submission processes.
- Excellent scientific writing, analytical, and problem-solving skills.
- Strong interpersonal and communication skills, with the ability to build effective relationships.
- Experience in (Specific Therapeutic Area, e.g., Oncology, Cardiology) is a plus.
- Proficiency in relevant clinical trial management systems and statistical software.
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1
Clinical Research Scientist
SW1A 0AA London, London
£65000 Annually
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Posted 2 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is looking for an innovative Clinical Research Scientist to contribute to groundbreaking drug development from the comfort of their home. This is a fully remote position, offering the flexibility to work from anywhere within the UK, with a focus on designing and executing clinical trials that will shape the future of medicine. You will be responsible for the scientific integrity of clinical studies, from protocol development through to final study report.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
Key responsibilities include analyzing complex data sets, interpreting results, and presenting findings to internal stakeholders and regulatory bodies. You will collaborate closely with cross-functional teams, including statisticians, medical writers, and regulatory affairs specialists, to ensure compliance with all relevant guidelines and regulations. This role demands a deep understanding of pharmaceutical research methodologies, statistical analysis, and regulatory requirements (e.g., GCP, ICH). A PhD or equivalent in a relevant life science discipline (e.g., pharmacology, biochemistry, molecular biology) is highly preferred, along with a proven track record of successfully managing clinical trials.
The ideal candidate will possess exceptional analytical skills, a meticulous attention to detail, and the ability to work independently with minimal supervision. Strong written and verbal communication skills are essential for documenting research, writing manuscripts for publication, and presenting scientific information clearly and concisely. You should be adept at managing multiple projects simultaneously and meeting tight deadlines. This is an exceptional opportunity to join a forward-thinking organization and make a significant impact on global health, working on cutting-edge therapies. Your expertise will be crucial in bringing life-changing treatments to patients worldwide. Embrace the future of pharmaceutical research in this exciting remote role.
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2
Clinical Research Scientist
NG1 1 Nottingham, East Midlands
£55000 Annually
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Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a highly skilled and motivated Clinical Research Scientist to join their innovative, fully remote research and development team. This crucial role will involve contributing to the design, execution, and analysis of clinical trials, with a focus on (Specific therapeutic area, e.g., oncology, immunology, rare diseases). You will be instrumental in advancing novel drug candidates through the development pipeline, from pre-clinical research to regulatory submission. The ideal candidate will possess a strong scientific background, meticulous attention to detail, and the ability to thrive in a fast-paced, virtual research environment. This is an exceptional opportunity to contribute to life-changing medical advancements from the comfort of your home.
Responsibilities:
Responsibilities:
- Contribute to the design and development of clinical trial protocols, ensuring scientific integrity and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, investigator meetings, and monitoring activities.
- Analyze and interpret complex clinical data, preparing comprehensive reports and presentations for internal stakeholders and regulatory agencies.
- Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management.
- Stay abreast of the latest scientific literature, emerging technologies, and regulatory guidelines relevant to clinical research.
- Contribute to the writing of investigational new drug (IND) applications, clinical study reports (CSRs), and manuscripts for publication.
- Identify and mitigate risks associated with clinical trial execution.
- Manage relationships with external collaborators, key opinion leaders (KOLs), and contract research organizations (CROs).
- Contribute to the development of scientific strategies and pipeline planning.
- Ensure all research activities are conducted in compliance with Good Clinical Practice (GCP) guidelines and company policies.
- Ph.D. or Master's degree in a relevant scientific discipline (e.g., life sciences, pharmacology, biomedical science).
- Minimum of 5 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
- Demonstrated experience in designing, conducting, and analyzing clinical trials.
- Strong understanding of drug development processes and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and data analysis skills.
- Proficiency in statistical software and data management systems is a plus.
- Exceptional communication, collaboration, and interpersonal skills.
- Ability to work independently, manage multiple projects simultaneously, and meet tight deadlines in a remote setting.
- Experience in (Specific therapeutic area) is highly desirable.
- Proven ability to critically evaluate scientific data and contribute to strategic decision-making.
- Must have a dedicated home office setup with reliable high-speed internet to perform duties effectively.
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3
Clinical Research Scientist - Oncology
NE1 4XX Newcastle upon Tyne, North East
£65000 Annually
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Posted 2 days ago
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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.
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4
Clinical Research Scientist - Oncology
LS1 1UR Leeds, Yorkshire and the Humber
£60000 Annually
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Posted 2 days ago
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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 .
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5
Clinical Research Scientist - Oncology
SO15 0AA Southampton, South East
£50000 Annually
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Posted 3 days ago
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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.
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Clinical Research Scientist - Oncology
CF10 1AA Cardiff, Wales
£55000 Annually
WhatJobs
Posted 3 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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7
Clinical Research Scientist - Oncology
NE1 7RU Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 3 days ago
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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.
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8
Clinical Research Scientist - Oncology
OX1 3PA Oxford, South East
£55000 Annually
WhatJobs
Posted 3 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.
This advertiser has chosen not to accept applicants from your region.
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