1,851 Oncology Research jobs in the United Kingdom
Clinical Research Scientist - Oncology
OX1 3PA Oxford, South East
£55000 Annually
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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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Clinical Research Scientist - Oncology
SW1A 0AA London, London
£70000 Annually
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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.
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Senior Clinical Research Scientist - Oncology
L3 9 Liverpool, North West
£65000 Annually
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Our client, a leading pharmaceutical innovator based in Liverpool, Merseyside, UK , is looking for a highly skilled Senior Clinical Research Scientist to spearhead critical oncology research initiatives. This role offers a unique opportunity to contribute to the development of groundbreaking therapies for cancer patients. The successful candidate will play a key role in the design, execution, and interpretation of early-phase clinical trials, focusing on novel oncology drug candidates. You will be responsible for developing study protocols, statistical analysis plans, and clinical study reports, ensuring adherence to regulatory guidelines and scientific rigor. This involves close collaboration with cross-functional teams, including R&D, regulatory affairs, clinical operations, and medical affairs. The Senior Clinical Research Scientist will contribute to the scientific strategy for oncology drug development, identify potential research opportunities, and assess the scientific merit of new targets and technologies. You will lead the scientific aspects of Investigator Meetings and present study data at scientific conferences and to key opinion leaders. A crucial part of the role involves staying abreast of the latest scientific literature, emerging research trends, and competitive landscape in oncology. You will be involved in the preparation of regulatory submissions (e.g., IND, CTA) and will serve as a subject matter expert for internal and external stakeholders. The ability to critically evaluate scientific data, design robust experiments, and communicate complex scientific information clearly and concisely is essential. This position requires a deep understanding of cancer biology, drug development processes, and clinical trial methodologies. Experience with statistical software and data analysis is necessary. The ideal candidate will possess strong leadership skills, a proactive approach to problem-solving, and the ability to mentor junior scientists. This is an exciting opportunity to make a tangible impact on patient lives by advancing innovative cancer treatments. Applicants should hold a PhD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) with substantial post-doctoral or industry experience in clinical research, specifically within oncology.
Responsibilities:
Responsibilities:
- Design and execute early-phase clinical trials in oncology.
- Develop study protocols, statistical analysis plans, and clinical study reports.
- Collaborate with multidisciplinary teams on oncology drug development strategy.
- Assess scientific merit of new targets and therapeutic approaches.
- Present study data at scientific conferences and to stakeholders.
- Stay current with oncology research, trends, and regulatory guidelines.
- Contribute to regulatory submissions and serve as a scientific subject matter expert.
- Critically evaluate scientific literature and research data.
- Mentor junior scientists and research staff.
- Foster strong relationships with key opinion leaders and external researchers.
- PhD in Oncology, Pharmacology, Molecular Biology, or a related field.
- Significant experience (e.g., 5+ years) in clinical research within the pharmaceutical industry or academic setting, with a focus on oncology.
- In-depth knowledge of cancer biology, immunotherapy, and targeted therapies.
- Proven ability to design and conduct clinical trials according to GCP guidelines.
- Experience with protocol development, data analysis, and reporting.
- Familiarity with regulatory submission processes (IND, CTA).
- Strong understanding of biostatistics and data interpretation.
- Excellent scientific writing and presentation skills.
- Demonstrated leadership and team collaboration abilities.
- Ability to critically analyze complex scientific data.
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Senior Clinical Research Scientist (Oncology)
CV1 2GT Coventry, West Midlands
£75000 Annually
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Our client, a pioneering pharmaceutical company at the forefront of developing groundbreaking cancer therapies, is seeking a highly accomplished Senior Clinical Research Scientist specializing in Oncology. This is a fully remote position, allowing you to contribute your expertise from anywhere in the UK. The successful candidate will play a critical role in the design, execution, and interpretation of clinical trials for novel oncology drugs. This involves deep engagement with study protocols, data analysis, regulatory submissions, and collaboration with internal and external stakeholders, including investigators, clinical research associates, and regulatory agencies. You will be responsible for ensuring the scientific integrity and successful progression of clinical development programs, contributing significantly to the advancement of patient care.
Key Responsibilities:
Key Responsibilities:
- Lead the scientific strategy and design of Phase I-IV clinical trials in oncology.
- Develop and refine clinical trial protocols, study plans, and statistical analysis plans.
- Oversee the execution of clinical trials, ensuring adherence to protocols, GCP, and regulatory requirements.
- Analyze and interpret complex clinical trial data, translating findings into actionable insights.
- Prepare scientific reports, publications, and presentations for internal review and external dissemination.
- Liaise with regulatory authorities (e.g., MHRA, EMA) regarding study submissions and approvals.
- Collaborate closely with cross-functional teams, including R&D, medical affairs, and commercial departments.
- Provide scientific and clinical expertise to investigators, study coordinators, and site staff.
- Contribute to the development of regulatory submission documents (e.g., IND, NDA).
- Stay abreast of the latest advancements in oncology research, clinical practice, and drug development.
- PhD or MD in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology) or equivalent experience.
- Minimum of 7 years of experience in clinical research and development within the pharmaceutical or biotechnology industry, with a focus on oncology.
- Proven track record in designing and managing complex clinical trials.
- In-depth knowledge of oncology therapeutic areas, disease mechanisms, and treatment paradigms.
- Strong understanding of Good Clinical Practice (GCP) and relevant regulatory guidelines.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Superb written and verbal communication skills, with experience in scientific writing and presentation.
- Demonstrated ability to collaborate effectively in a remote, multi-disciplinary team environment.
- Experience with data analysis and interpretation, including statistical concepts.
- Eligibility to work remotely within the UK.
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Lead Clinical Research Scientist - Oncology
Cambridge CB2 1TN Cambridge, Eastern
£70000 Annually
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Posted 1 day ago
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Our client, a world-renowned biotechnology company at the forefront of medical innovation, is seeking a highly skilled and motivated Lead Clinical Research Scientist to join their oncology R&D division. This hybrid role is central to advancing our understanding and treatment of cancer through rigorous scientific investigation. You will be responsible for designing, executing, and interpreting complex clinical research studies, contributing to the development of novel therapeutic agents. This involves developing research protocols, collaborating with clinical operations teams, analysing study data, and contributing to scientific publications and regulatory submissions. The ideal candidate will possess a PhD or equivalent in a relevant life science discipline (e.g., oncology, immunology, molecular biology), with a minimum of 7 years of experience in clinical research within the pharmaceutical or biotechnology industry. Proven experience in oncology drug development and a deep understanding of clinical trial methodologies are essential. You should have a strong track record of scientific achievement, including publications in peer-reviewed journals and presentations at scientific conferences. Responsibilities include providing scientific leadership, mentoring junior research staff, and collaborating effectively with internal and external stakeholders, including investigators, key opinion leaders, and regulatory agencies. Excellent written and verbal communication skills are critical for disseminating research findings and influencing scientific direction. This hybrid position requires a balance of remote data analysis and scientific writing with in-office collaboration at our **Cambridge** research campus, fostering a dynamic and innovative environment. You will play a key role in shaping the future of cancer therapy.
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4
Senior Clinical Research Scientist (Oncology)
NG1 1BB Nottingham, East Midlands
£70000 Annually
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Posted 2 days ago
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Our client, a prominent pharmaceutical research organization, is seeking a highly motivated Senior Clinical Research Scientist specializing in Oncology. This role operates on a hybrid model, offering a blend of remote flexibility and essential in-office engagement at our Nottingham, Nottinghamshire, UK facility.
The successful candidate will play a crucial role in the design, execution, and interpretation of clinical trials for novel oncology therapeutics. You will contribute to all phases of clinical development, from protocol design and site selection to data analysis and regulatory submissions. This position requires a strong scientific background, in-depth knowledge of oncology, and excellent project management skills.
Key Responsibilities:
The successful candidate will play a crucial role in the design, execution, and interpretation of clinical trials for novel oncology therapeutics. You will contribute to all phases of clinical development, from protocol design and site selection to data analysis and regulatory submissions. This position requires a strong scientific background, in-depth knowledge of oncology, and excellent project management skills.
Key Responsibilities:
- Design and develop clinical trial protocols, investigator brochures, and other study-related documents.
- Oversee the operational aspects of clinical trials, ensuring compliance with GCP, regulatory guidelines, and study objectives.
- Collaborate with cross-functional teams, including medical affairs, R&D, regulatory affairs, and clinical operations.
- Manage relationships with clinical sites, investigators, and key opinion leaders.
- Contribute to the analysis and interpretation of clinical trial data, including statistical analysis.
- Prepare clinical study reports (CSRs) and contribute to scientific publications and presentations.
- Evaluate new drug candidates and therapeutic strategies for potential development.
- Ensure the safety and well-being of study participants throughout the trial.
- Participate in regulatory interactions and submissions.
- Mentor junior research scientists and provide scientific guidance.
- Stay abreast of the latest advancements in oncology research and clinical trial methodologies.
- PhD or PharmD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biochemistry, Medicine).
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a strong focus on oncology.
- Proven experience in clinical trial design, execution, and data interpretation.
- In-depth knowledge of oncology, including current treatment paradigms and emerging therapeutic areas.
- Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing, analytical, and communication skills.
- Demonstrated ability to work effectively in a hybrid work environment, managing remote collaboration and in-office responsibilities.
- Strong project management skills and the ability to manage multiple priorities.
- Experience with statistical analysis of clinical data is desirable.
- Ability to work independently and as part of a collaborative team.
- A passion for advancing cancer treatment and improving patient outcomes.
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Principal Clinical Research Scientist - Oncology
CV1 2DT Coventry, West Midlands
£75000 Annually
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Posted 2 days ago
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Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is seeking a highly experienced and accomplished Principal Clinical Research Scientist to lead critical research initiatives in Oncology. Based in Coventry, West Midlands, UK , this role offers a unique opportunity to shape the future of cancer treatment. You will be instrumental in the design, execution, and interpretation of complex clinical trials, driving the development of novel therapies from early-stage research through to regulatory submission.
Responsibilities include developing clinical trial protocols, defining study objectives and endpoints, and selecting appropriate patient populations. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure the successful conduct of studies. The Principal Clinical Research Scientist will also be responsible for evaluating research data, analysing results, and preparing scientific publications and presentations for key conferences and regulatory agencies. Strong scientific acumen, a deep understanding of oncology, and a proven ability to interpret complex biological and clinical data are essential.
The ideal candidate will hold a PhD or equivalent in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) and possess extensive experience in clinical trial management and drug development within the pharmaceutical industry. You should have a comprehensive understanding of ICH-GCP guidelines, regulatory requirements, and drug development processes. Exceptional leadership, communication, and project management skills are crucial, as you will be guiding research strategies and mentoring junior scientists. This role requires a strategic thinker with a passion for advancing patient care through scientific excellence.
Key Responsibilities:
This hybrid role offers a competitive salary, comprehensive benefits package, and the opportunity to make a significant impact on the lives of patients. If you are a visionary scientist with a passion for oncology drug development, we encourage you to apply.
Responsibilities include developing clinical trial protocols, defining study objectives and endpoints, and selecting appropriate patient populations. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure the successful conduct of studies. The Principal Clinical Research Scientist will also be responsible for evaluating research data, analysing results, and preparing scientific publications and presentations for key conferences and regulatory agencies. Strong scientific acumen, a deep understanding of oncology, and a proven ability to interpret complex biological and clinical data are essential.
The ideal candidate will hold a PhD or equivalent in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology) and possess extensive experience in clinical trial management and drug development within the pharmaceutical industry. You should have a comprehensive understanding of ICH-GCP guidelines, regulatory requirements, and drug development processes. Exceptional leadership, communication, and project management skills are crucial, as you will be guiding research strategies and mentoring junior scientists. This role requires a strategic thinker with a passion for advancing patient care through scientific excellence.
Key Responsibilities:
- Design and develop innovative clinical trial protocols for oncology therapeutics.
- Oversee the execution of clinical studies, ensuring adherence to protocols and regulatory standards.
- Analyse and interpret complex clinical trial data, translating findings into actionable insights.
- Prepare scientific manuscripts, abstracts, and presentations for publication and dissemination.
- Collaborate with internal and external stakeholders, including investigators, KOLS, and regulatory bodies.
- Provide scientific and strategic leadership for oncology drug development programs.
- Contribute to regulatory submissions and responses to health authorities.
- Evaluate emerging scientific literature and research trends in oncology.
- Mentor and guide junior research scientists and clinical study personnel.
- Manage research budgets and project timelines effectively.
This hybrid role offers a competitive salary, comprehensive benefits package, and the opportunity to make a significant impact on the lives of patients. If you are a visionary scientist with a passion for oncology drug development, we encourage you to apply.
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Senior Clinical Research Scientist - Oncology
G1 1DU Glasgow, Scotland
£70000 Annually
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Posted 3 days ago
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Our client, a global leader in pharmaceutical innovation, is seeking a highly experienced Senior Clinical Research Scientist specializing in Oncology to join their fully remote team. This critical role involves contributing to the design, development, and execution of cutting-edge clinical trials for novel cancer therapies. You will play a key part in translating scientific discoveries into life-saving treatments, working closely with cross-functional teams to ensure the highest standards of research integrity and patient safety. This is an excellent opportunity for a dedicated scientist to drive impactful research from the convenience of their home office.
Key Responsibilities:
Key Responsibilities:
- Contribute to the design and development of clinical trial protocols, ensuring scientific rigor and alignment with regulatory requirements.
- Provide scientific and clinical expertise throughout the lifecycle of clinical trials, from initiation to database lock.
- Collaborate with investigators, study coordinators, and internal teams to ensure effective trial execution and data integrity.
- Analyze and interpret complex clinical data, contributing to the scientific evaluation of study results.
- Prepare scientific documents, including clinical study reports, regulatory submissions, and publications.
- Stay abreast of the latest advancements in oncology research, clinical practice, and regulatory guidelines.
- Mentor and provide scientific guidance to junior colleagues and external study teams.
- Participate in scientific meetings, conferences, and advisory boards.
- Ensure compliance with all applicable regulatory standards (e.g., ICH-GCP) and company policies.
- Contribute to the strategic planning of the oncology pipeline and therapeutic area development.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Biology, Medicine).
- Extensive experience (5+ years) in clinical research within the pharmaceutical industry, with a strong focus on oncology.
- Deep understanding of clinical trial design, execution, and data analysis.
- Proven ability to interpret complex clinical data and contribute to scientific publications.
- Excellent knowledge of oncology therapeutic areas and the drug development process.
- Strong scientific writing and communication skills.
- Ability to collaborate effectively with diverse, geographically dispersed teams in a remote setting.
- Experience with regulatory submissions and interactions with health authorities.
- Proficiency in scientific literature review and critical evaluation.
- A passion for advancing cancer care and improving patient outcomes.
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7
Senior Clinical Research Scientist - Oncology
DE1 0AA Derby, East Midlands
£75000 Annually
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Posted 4 days ago
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Our client, a renowned pharmaceutical company at the forefront of medical innovation, is seeking a highly motivated and experienced Senior Clinical Research Scientist with a specialization in Oncology to join their remote-based research team. This critical role will contribute to the design, execution, and analysis of clinical trials for novel cancer therapies. The successful candidate will be instrumental in developing study protocols, selecting and managing clinical sites, and ensuring compliance with regulatory guidelines (e.g., GCP, FDA, EMA). Responsibilities include critically evaluating scientific literature, interpreting complex clinical data, and authoring regulatory submissions and scientific publications. You will collaborate closely with cross-functional teams, including biostatistics, data management, regulatory affairs, and medical affairs, to ensure the seamless progression of research projects. This is a remote position, requiring exceptional organisational skills, independent work ethic, and advanced virtual communication capabilities. The ability to effectively manage multiple projects simultaneously, build strong relationships with external investigators and key opinion leaders, and adapt to evolving research landscapes is paramount. A strong understanding of oncology disease areas, drug development processes, and statistical methodologies is essential. You will play a key role in advancing our client's pipeline of life-saving treatments. A PhD or MD in a relevant life science discipline, coupled with a minimum of 6 years of experience in clinical research within the pharmaceutical or biotechnology industry, is required. Experience specifically in oncology clinical trials is a mandatory requirement.
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Senior Clinical Research Scientist - Oncology
SO14 0AA Southampton, South East
£70000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical company dedicated to advancing cancer research and developing novel oncology treatments, is seeking an experienced Senior Clinical Research Scientist to join their fully remote scientific team. This role is pivotal in driving the design, execution, and interpretation of clinical trials aimed at bringing life-changing therapies to patients. You will play a key role in the strategic planning of clinical development programs, contributing scientific expertise and leadership from early-phase studies through to regulatory submission. Key responsibilities include developing clinical trial protocols, designing study endpoints, and selecting appropriate biomarkers. You will collaborate closely with internal R&D departments, external investigators, and regulatory agencies to ensure the scientific integrity and success of clinical studies. This includes analysing clinical trial data, preparing scientific publications, and presenting findings at key scientific forums. The ideal candidate will possess a PhD or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology), with a strong track record in clinical research within the pharmaceutical industry. Deep knowledge of oncology drug development, clinical trial methodologies, and regulatory requirements (e.g., FDA, EMA) is essential. Exceptional scientific acumen, analytical skills, and the ability to critically evaluate complex data are required. Strong communication and interpersonal skills are vital for effective collaboration with diverse teams and external partners. This is a unique opportunity to contribute significantly to the fight against cancer, working remotely with a world-class organisation that has a strong presence and research focus, including in the **Southampton, Hampshire, UK**, region and beyond.
Key Responsibilities:
Key Responsibilities:
- Contribute to the strategic design and development of oncology clinical trial protocols.
- Provide scientific and clinical expertise throughout the drug development lifecycle.
- Define clinical development plans, study objectives, and endpoints.
- Collaborate with cross-functional teams, including R&D, regulatory affairs, and medical affairs.
- Liaise with principal investigators and clinical trial sites to ensure protocol compliance.
- Analyse and interpret clinical trial data, including biomarker data.
- Prepare scientific reports, manuscripts for publication, and regulatory submission documents.
- Present clinical trial results at scientific meetings and conferences.
- Stay abreast of the latest advancements in oncology research and clinical development.
- Mentor junior scientists and contribute to the scientific knowledge base of the organization.
- PhD or MD in Oncology, Pharmacology, Molecular Biology, or a related life science field.
- Significant experience in clinical research and drug development within the pharmaceutical or biotech industry.
- In-depth knowledge of oncology indications, therapeutic areas, and clinical trial design.
- Proven experience in protocol development, data analysis, and scientific writing.
- Familiarity with global regulatory requirements (e.g., ICH-GCP, FDA, EMA).
- Excellent analytical, critical thinking, and problem-solving skills.
- Outstanding verbal and written communication skills.
- Ability to work independently and collaboratively in a remote scientific setting.
- Strong project management and organizational abilities.
- A passion for advancing cancer treatment and improving patient outcomes.
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