362 Oncology jobs in the United Kingdom
Clinical Oncology Consultant
Derby, East Midlands
£60000 - £90000 annum
Hope Homecare Services Limited
Posted 155 days ago
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Job Description
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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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0
Clinical Research Scientist (Oncology)
PO1 1AA Portsmouth, South East
£50000 Annually
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Our client, a leading pharmaceutical innovator, is seeking a highly skilled Clinical Research Scientist specializing in Oncology to join their dedicated team. This role offers a unique opportunity to contribute to the development of life-saving therapies, working within a hybrid model that balances essential in-office collaboration with remote flexibility. You will play a crucial role in the design, execution, and analysis of clinical trials, ensuring the highest standards of scientific integrity and regulatory compliance. The ideal candidate possesses a deep understanding of oncology drug development, strong analytical capabilities, and a passion for advancing patient care.
Key Responsibilities:
Qualifications:
This hybrid role offers the flexibility of remote work combined with essential in-office collaboration, based at our client's facility in Portsmouth, Hampshire, UK . Join a team dedicated to making a significant difference in the lives of cancer patients worldwide.
Key Responsibilities:
- Design and develop clinical trial protocols for oncology indications, ensuring scientific validity and alignment with strategic objectives.
- Oversee the operational aspects of clinical trials, including site selection, investigator training, and data monitoring.
- Analyze and interpret complex clinical trial data, preparing comprehensive reports for regulatory submissions and internal stakeholders.
- Collaborate closely with cross-functional teams, including R&D, regulatory affairs, medical affairs, and project management.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements.
- Evaluate and present scientific findings at internal meetings, advisory boards, and external conferences.
- Contribute to the development of new drug candidates and the optimization of existing treatments.
- Manage relationships with external investigators, key opinion leaders, and contract research organizations (CROs).
- Stay abreast of the latest advancements in oncology research, clinical trial methodologies, and regulatory landscapes.
- Contribute to the scientific and strategic direction of the oncology pipeline.
Qualifications:
- Ph.D. or M.D. in a relevant scientific or medical field, with a strong focus on oncology.
- Minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry.
- Demonstrated expertise in designing, conducting, and analyzing Phase I-III clinical trials for oncology drugs.
- In-depth knowledge of oncology biology, disease mechanisms, and therapeutic strategies.
- Familiarity with regulatory requirements (FDA, EMA) and ICH/GCP guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
- Experience in managing external collaborations and CROs.
- Ability to work effectively in a hybrid work environment, balancing remote and in-office responsibilities.
- A proactive approach and a passion for contributing to groundbreaking medical advancements.
This hybrid role offers the flexibility of remote work combined with essential in-office collaboration, based at our client's facility in Portsmouth, Hampshire, UK . Join a team dedicated to making a significant difference in the lives of cancer patients worldwide.
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Clinical Research Scientist (Oncology)
M17 8 Manchester, North West
£55000 Annually
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Posted today
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A leading pharmaceutical company based in Manchester, Greater Manchester, UK , is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their innovative research and development team. This is a Hybrid role, combining the flexibility of remote work with the collaborative environment of our state-of-the-art facility. You will play a critical role in the design, execution, and interpretation of clinical trials for novel cancer therapies.
Responsibilities include developing clinical trial protocols, selecting and managing clinical sites, overseeing data collection and analysis, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to drive research objectives forward. The ideal candidate will have a strong scientific background with expertise in oncology drug development. You will be involved in identifying potential patient populations, assessing drug safety and efficacy, and contributing to regulatory submissions. This position demands meticulous attention to detail, exceptional analytical skills, and the ability to communicate complex scientific information effectively.
Qualifications include a PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related discipline, with a minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotech industry, specifically in oncology. Proven experience in designing and managing Phase I-III clinical trials is essential. Knowledge of cancer biology, therapeutic targets, and current treatment landscapes is required. Excellent written and verbal communication skills, strong project management abilities, and the capacity to work independently as well as part of a collaborative team are crucial. You should be adept at interpreting clinical data, preparing scientific reports, and presenting findings to internal and external stakeholders. This role offers a unique opportunity to contribute to the development of life-saving treatments and advance your career in a rapidly growing field.
Responsibilities include developing clinical trial protocols, selecting and managing clinical sites, overseeing data collection and analysis, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to drive research objectives forward. The ideal candidate will have a strong scientific background with expertise in oncology drug development. You will be involved in identifying potential patient populations, assessing drug safety and efficacy, and contributing to regulatory submissions. This position demands meticulous attention to detail, exceptional analytical skills, and the ability to communicate complex scientific information effectively.
Qualifications include a PhD or Master's degree in Life Sciences, Pharmacy, Medicine, or a related discipline, with a minimum of 3-5 years of experience in clinical research within the pharmaceutical or biotech industry, specifically in oncology. Proven experience in designing and managing Phase I-III clinical trials is essential. Knowledge of cancer biology, therapeutic targets, and current treatment landscapes is required. Excellent written and verbal communication skills, strong project management abilities, and the capacity to work independently as well as part of a collaborative team are crucial. You should be adept at interpreting clinical data, preparing scientific reports, and presenting findings to internal and external stakeholders. This role offers a unique opportunity to contribute to the development of life-saving treatments and advance your career in a rapidly growing field.
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2
Clinical Research Associate - Oncology
PL1 2EU Plymouth, South West
£40000 Annually
WhatJobs
Posted 1 day ago
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Our client, a prominent pharmaceutical company, is actively seeking a dedicated and experienced Clinical Research Associate (CRA) to support their vital oncology research program based in **Plymouth, Devon, UK**. This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. The CRA will be responsible for site monitoring, data verification, and fostering strong relationships with investigative sites and study teams to facilitate the efficient progress of clinical studies.
Key Responsibilities:
The successful candidate will hold a Bachelor's degree in a life science, nursing, or related field, or possess equivalent practical experience. A minimum of 2-3 years of direct experience as a Clinical Research Associate, with a strong focus on oncology trials, is required. Comprehensive knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical trials is essential. Demonstrated experience in site monitoring, data review, and regulatory documentation is expected. Excellent organizational, time management, and problem-solving skills are critical. Strong written and verbal communication abilities, along with excellent interpersonal skills to build rapport with site personnel, are paramount. The ability to travel to investigative sites as needed is a requirement for this role. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This is an excellent opportunity for a motivated CRA to contribute to significant advancements in cancer treatment.
Key Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits in accordance with protocol and company standard operating procedures.
- Ensure that clinical trials are conducted, recorded, and reported in compliance with the protocol, standard operating procedures, and applicable regulatory requirements (e.g., GCP, ICH).
- Verify the accuracy and completeness of source data and clinical trial documentation through source data verification (SDV).
- Manage and resolve data queries and discrepancies in a timely manner.
- Serve as the primary point of contact for assigned investigative sites, addressing issues and providing guidance to site staff.
- Ensure drug accountability and investigational product management at study sites.
- Maintain accurate and up-to-date trial documentation in the Trial Master File (TMF).
- Communicate effectively with investigators, study coordinators, and internal study team members.
- Identify, document, and escalate any site-related issues or risks to the Clinical Trial Manager or other relevant personnel.
- Participate in study team meetings and contribute to the overall success of the clinical trial.
The successful candidate will hold a Bachelor's degree in a life science, nursing, or related field, or possess equivalent practical experience. A minimum of 2-3 years of direct experience as a Clinical Research Associate, with a strong focus on oncology trials, is required. Comprehensive knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical trials is essential. Demonstrated experience in site monitoring, data review, and regulatory documentation is expected. Excellent organizational, time management, and problem-solving skills are critical. Strong written and verbal communication abilities, along with excellent interpersonal skills to build rapport with site personnel, are paramount. The ability to travel to investigative sites as needed is a requirement for this role. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This is an excellent opportunity for a motivated CRA to contribute to significant advancements in cancer treatment.
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3
Clinical Research Scientist - Oncology
PL1 2LU Plymouth, South West
£50000 Annually
WhatJobs
Posted 4 days ago
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Our client, a prominent pharmaceutical company, is seeking a dedicated and experienced Clinical Research Scientist specializing in Oncology to join their esteemed research and development team in Plymouth, Devon, UK . This critical role will focus on the design, implementation, and management of clinical trials for novel oncology therapeutics. The successful candidate will play a key role in advancing our understanding of cancer treatments and bringing life-saving medications to patients. Responsibilities include developing clinical trial protocols, overseeing patient recruitment, managing data integrity, and ensuring compliance with regulatory guidelines (e.g., GCP, ICH). You will collaborate closely with investigators, site staff, and internal cross-functional teams, including medical affairs, regulatory affairs, and project management. A strong understanding of oncology, including various cancer types, treatment modalities, and current research trends, is essential. Experience in analyzing clinical trial data, interpreting results, and contributing to scientific publications and regulatory submissions is highly desirable. The ideal candidate possesses excellent scientific acumen, meticulous attention to detail, and superior organizational and communication skills. This position offers a unique opportunity to contribute to groundbreaking research in a challenging and rewarding field. The role demands a commitment to scientific excellence and a passion for improving patient outcomes. You will be instrumental in shaping the clinical development strategy for our pipeline assets. Join a forward-thinking organization dedicated to making a real difference in the lives of cancer patients worldwide. The role is based at our facilities in Plymouth, Devon, UK , offering a stimulating work environment with opportunities for professional growth and development. This is a hands-on role requiring active participation in all phases of clinical trial execution.
Responsibilities:
Responsibilities:
- Develop and write clinical trial protocols and amendments.
- Contribute to the design and planning of Phase I-IV clinical trials in oncology.
- Monitor clinical trial progress and ensure adherence to protocols and regulatory requirements.
- Manage relationships with clinical investigators and site personnel.
- Oversee data collection, quality control, and analysis of clinical trial data.
- Contribute to the preparation of clinical study reports, scientific publications, and regulatory submissions.
- Provide scientific and clinical input to other functional areas.
- Stay updated on the latest scientific advancements and competitive landscape in oncology.
- Participate in the selection and management of external vendors and partners.
- Ensure ethical conduct and patient safety throughout the trial lifecycle.
- PhD or MSc in a life science discipline (e.g., Biology, Biochemistry, Pharmacology, Medicine).
- Minimum of 5 years of experience in clinical research, with a significant focus on oncology drug development.
- In-depth knowledge of oncology, clinical trial design, and regulatory requirements.
- Strong understanding of Good Clinical Practice (GCP) and ICH guidelines.
- Proven ability to analyze and interpret clinical data.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects and prioritize effectively.
- Strong interpersonal skills and ability to work collaboratively in a team environment.
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Clinical Research Scientist - Oncology
NE1 1 Newcastle upon Tyne, North East
£55000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking an exceptional Clinical Research Scientist specializing in Oncology to join their innovative R&D team based near Newcastle upon Tyne, Tyne and Wear, UK . This hybrid role offers the best of both worlds, combining essential on-site collaboration with the flexibility of remote work. You will be instrumental in designing, conducting, and analyzing clinical trials for novel cancer therapies, contributing significantly to the advancement of patient care. The ideal candidate will possess a strong scientific background, a deep understanding of oncology drug development, and a passion for cutting-edge research.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology therapeutics, ensuring scientific rigor and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, investigator meetings, and monitoring trial progress.
- Analyze and interpret complex clinical data, preparing comprehensive reports and scientific publications.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, and project management, to ensure seamless trial operations.
- Identify and evaluate potential drug targets and biomarkers for new oncology treatments.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Stay abreast of the latest advancements in oncology, clinical research methodologies, and pharmaceutical regulations.
- Present research findings at scientific conferences and internal meetings.
- Mentor junior research staff and contribute to the development of the research team.
- Ensure adherence to Good Clinical Practice (GCP) and other relevant ethical guidelines.
- Ph.D. or M.D. in a relevant life science discipline (e.g., Oncology, Pharmacology, Molecular Biology).
- Minimum of 4-6 years of experience in clinical research, with a focus on oncology drug development.
- Proven track record in designing and managing complex clinical trials.
- In-depth knowledge of cancer biology, therapeutic modalities, and current treatment landscape.
- Experience with statistical analysis of clinical data and familiarity with biostatistics principles.
- Excellent scientific writing and presentation skills.
- Strong understanding of regulatory requirements (FDA, EMA) and GCP guidelines.
- Ability to work effectively in a collaborative, cross-functional team environment.
- Experience with hybrid work models and proficient in remote collaboration tools.
- Demonstrated ability to think critically and solve complex scientific problems.
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5
Clinical Research Scientist (Oncology)
WV1 1AB Wolverhampton, West Midlands
£55000 Annually
WhatJobs
Posted 8 days ago
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Our client, a prominent pharmaceutical company, is seeking an accomplished Clinical Research Scientist specializing in Oncology to join their dedicated research team based in **Wolverhampton, West Midlands, UK**. This is a vital on-site role focused on the design, execution, and monitoring of clinical trials for innovative oncology therapeutics. The successful candidate will play a crucial part in bringing life-changing treatments to patients by ensuring trials are conducted ethically, efficiently, and in compliance with global regulatory standards. You will work closely with investigators, clinical research associates, and internal stakeholders to manage all aspects of clinical trial operations.
Key Responsibilities:
Key Responsibilities:
- Contribute to the development of clinical trial protocols and study designs for oncology indications.
- Oversee the initiation, conduct, and completion of clinical trials at assigned investigational sites.
- Ensure adherence to Good Clinical Practice (GCP), regulatory requirements, and company SOPs.
- Manage relationships with investigators, site staff, and contract research organizations (CROs).
- Monitor trial progress, data quality, and patient safety, implementing corrective actions as needed.
- Review and interpret clinical data, preparing reports on study progress and outcomes.
- Collaborate with medical affairs, regulatory affairs, and R&D teams to ensure seamless trial management.
- Contribute to the preparation of regulatory submissions and scientific publications.
- Identify and assess potential risks and develop mitigation strategies for clinical trials.
- Provide scientific and operational guidance to clinical research associates (CRAs) and other study personnel.
- Maintain accurate and comprehensive trial documentation.
- Participate in site selection and initiation visits.
- Ph.D. or Master's degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Minimum of 5 years of experience in clinical research, with a significant focus on oncology trials.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in managing clinical trials from protocol development through to final study report.
- Excellent understanding of oncology, including disease states, therapeutic approaches, and drug development processes.
- Strong project management and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work effectively under pressure and manage multiple priorities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel to clinical sites as required.
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6
Clinical Research Scientist - Oncology
NG1 4GE Nottingham, East Midlands
£65000 Annually
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Posted 10 days ago
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Our client, a cutting-edge biomedical research organization, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology to join their fully remote research and development team. This critical role will involve contributing to the design, execution, and analysis of groundbreaking clinical trials aimed at developing novel cancer therapies. You will be instrumental in translating preclinical findings into clinical applications and advancing our understanding of cancer biology and treatment. The position requires a deep scientific background, extensive experience in oncology research, and a passion for making a difference in patient lives. As part of a remote-first organization, you will collaborate virtually with a team of world-class scientists, clinicians, and statisticians. Key responsibilities include protocol development, data interpretation, scientific writing (publications, reports, regulatory submissions), and staying abreast of the latest scientific literature and technological advancements in oncology. You will critically evaluate research data, design experiments, and contribute to the strategic direction of our oncology pipeline. The ideal candidate will have a Ph.D. in a relevant biomedical science discipline (e.g., molecular biology, immunology, pharmacology) with a strong focus on cancer research. Proven experience in clinical trial design and execution, including knowledge of regulatory guidelines (e.g., ICH-GCP), is essential. Exceptional analytical, problem-solving, and communication skills are required, as is the ability to thrive in an independent, self-directed remote work environment. We are looking for a scientist who is not only technically proficient but also possesses strong scientific curiosity and a collaborative spirit. This is an unparalleled opportunity to contribute to transformative cancer research and development from the comfort of your home, working with leading experts in the field. Your insights will directly influence the trajectory of life-saving treatments and therapies. The role demands a high level of scientific rigor and ethical conduct, ensuring the integrity of all research activities. You will be a key player in bringing innovative solutions to patients facing cancer worldwide. This position offers significant opportunities for professional growth and the chance to be at the forefront of oncological advancements.
Responsibilities:
Responsibilities:
- Contribute to the design and execution of oncology clinical trials.
- Analyze and interpret complex clinical data, identifying key trends and insights.
- Author scientific publications, presentations, and regulatory documents.
- Collaborate with cross-functional teams, including medical affairs, statistics, and regulatory affairs.
- Stay current with scientific literature, emerging technologies, and competitive landscape in oncology.
- Provide scientific expertise and support for ongoing and planned clinical studies.
- Contribute to the strategic planning and development of the oncology pipeline.
- Ensure adherence to all relevant ethical and regulatory guidelines (e.g., ICH-GCP).
- Ph.D. in Molecular Biology, Immunology, Pharmacology, Oncology, or a related biomedical science.
- Minimum of 5 years of post-doctoral or industry experience in oncology drug development and clinical research.
- Strong understanding of cancer biology, mechanisms of action, and therapeutic strategies.
- Experience with clinical trial design, data analysis, and interpretation.
- Excellent scientific writing and presentation skills.
- Proficiency in statistical analysis software and data management tools is a plus.
- Demonstrated ability to work independently and collaboratively in a remote setting.
- Strong critical thinking, problem-solving, and organizational skills.
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7
Clinical Research Scientist - Oncology
BD3 7ES Bradford, Yorkshire and the Humber
£45000 Annually
WhatJobs
Posted 12 days ago
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Our client, a leading pharmaceutical company, is seeking a dedicated and highly skilled Clinical Research Scientist to join their Oncology research team in Bradford, West Yorkshire, UK . This role is integral to the development and execution of innovative clinical trials aimed at combating cancer. You will be responsible for designing, implementing, and monitoring clinical studies, ensuring adherence to ethical guidelines, regulatory requirements, and scientific integrity. The ideal candidate will possess a strong background in oncology, clinical research methodologies, and data analysis. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, biostatistics, and project management, to advance drug development programs. Key responsibilities include developing study protocols, overseeing site selection and initiation, managing data collection and analysis, and ensuring the safety and well-being of trial participants. You will also contribute to the interpretation of study results and the preparation of regulatory submissions and scientific publications. This position demands excellent scientific acumen, critical thinking, and robust project management skills. The ability to communicate complex scientific information clearly and concisely, both verbally and in writing, is essential. We are looking for a proactive and meticulous researcher who is passionate about making a difference in the lives of cancer patients. Your contributions will be vital in bringing novel therapies to market and advancing the field of oncology. We offer a stimulating work environment, opportunities for professional growth, and the chance to work on cutting-edge pharmaceutical research. This is an exciting opportunity to be at the forefront of cancer drug development in Bradford . We value individuals who are driven by scientific curiosity and a commitment to improving patient outcomes. Your role will involve close interaction with clinical investigators, study sites, and internal R&D teams to ensure the successful progression of research projects. We are committed to scientific excellence and ethical conduct throughout our clinical research endeavors. Join our esteemed team and contribute to significant advancements in cancer treatment.
Responsibilities:
Responsibilities:
- Design and develop clinical trial protocols in oncology.
- Oversee the execution and monitoring of clinical studies.
- Ensure compliance with GCP, ICH guidelines, and relevant regulatory requirements.
- Collaborate with cross-functional teams, including R&D, regulatory, and biostatistics.
- Manage relationships with clinical investigators and study sites.
- Oversee data collection, management, and analysis for clinical trials.
- Interpret study results and contribute to scientific publications and presentations.
- Contribute to the preparation of regulatory submissions (e.g., IND, NDA).
- Ensure the safety and ethical conduct of all clinical research activities.
- Stay abreast of scientific advancements and trends in oncology research.
- PhD or equivalent degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Significant experience in clinical research, with a focus on oncology.
- In-depth knowledge of clinical trial design, GCP, and regulatory requirements.
- Proven ability to manage complex clinical research projects.
- Excellent scientific writing, data analysis, and interpretation skills.
- Strong communication, interpersonal, and teamwork abilities.
- Proficiency in clinical trial management software and data analysis tools.
- Ability to work independently and contribute effectively in a team environment.
- Experience with pharmaceutical drug development processes.
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8
Clinical Research Scientist (Oncology)
BS1 6EH Bristol, South West
£60000 Annually
WhatJobs
Posted 16 days ago
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Our client, a leading global pharmaceutical company with a significant presence in **Bristol, South West England, UK**, is actively seeking a talented Clinical Research Scientist specializing in Oncology. This role adopts a hybrid working model, combining essential laboratory and team-based work at our state-of-the-art Bristol facility with the flexibility of remote work for data analysis and report writing. The Clinical Research Scientist will be instrumental in the design, execution, and analysis of clinical trials for novel oncology therapeutics. Responsibilities include developing study protocols, managing investigator-initiated studies, analyzing clinical data, interpreting results, and contributing to regulatory submissions. You will collaborate extensively with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external investigators, clinicians, and key opinion leaders. The ideal candidate will possess a PhD or equivalent in a relevant life science discipline (e.g., Molecular Biology, Pharmacology, Immunology) with a strong track record of successful clinical research in oncology. Excellent understanding of clinical trial methodologies, regulatory guidelines (e.g., ICH-GCP), and biostatistics is required. Strong written and verbal communication skills are paramount for scientific reporting and stakeholder engagement. This is a vital role contributing to the development of life-saving cancer treatments, offering a stimulating research environment and significant career development opportunities within a leading pharmaceutical organization.
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