6,985 Cancer Research jobs in the United Kingdom
Clinical Research Scientist
Posted today
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The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine) with a strong foundation in clinical research methodologies. You should have demonstrable experience in clinical trial management, including protocol development and study execution, within the pharmaceutical or biotechnology sector. A thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., EMA, FDA) is essential. Excellent analytical, problem-solving, and communication skills are required, along with the ability to present complex scientific information clearly and concisely. Experience with statistical analysis software and data visualization tools is advantageous. While this role is primarily based in our Manchester office, a hybrid work model allows for a balanced approach to on-site collaboration and remote work, offering flexibility for the right candidate.
Clinical Research Scientist
Posted 15 days ago
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Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific rigor, regulatory compliance, and alignment with study objectives.
- Oversee the execution of clinical trials, providing scientific and operational guidance to study teams.
- Analyze and interpret complex clinical data, drawing meaningful conclusions and preparing comprehensive study reports.
- Collaborate closely with cross-functional teams, including regulatory affairs, data management, biostatistics, and medical affairs.
- Contribute to the development of Investigator's Brochures, study manuals, and other essential study documents.
- Monitor study progress, identify potential issues, and implement corrective actions to ensure timely and high-quality trial completion.
- Stay current with scientific literature, emerging technologies, and regulatory guidelines relevant to clinical research.
- Present study findings at scientific meetings and contribute to publications in peer-reviewed journals.
- Manage relationships with external partners, including investigators, research sites, and contract research organizations (CROs).
- Ensure adherence to Good Clinical Practice (GCP) and other applicable regulatory standards.
- Provide scientific input into portfolio strategy and target product profiles.
- Evaluate potential new drug candidates and therapeutic areas for clinical development.
Qualifications:
- PhD or equivalent advanced degree in Life Sciences, Pharmacology, Medicine, or a related field.
- Minimum of 6-8 years of progressive experience in clinical research, with a strong focus on drug development within the pharmaceutical or biotechnology industry.
- Demonstrated success in designing and executing clinical trials across various therapeutic areas.
- Expertise in clinical data analysis, interpretation, and reporting.
- Thorough understanding of ICH guidelines, GCP, and relevant regulatory requirements (e.g., FDA, EMA).
- Excellent scientific writing and presentation skills.
- Proven ability to work effectively in a remote, collaborative, and international team environment.
- Strong project management and organizational skills.
- Experience with statistical analysis and interpretation of clinical trial data.
- Proficiency in using clinical trial management systems and electronic data capture (EDC) systems.
- Ability to critically evaluate scientific literature and data.
- A passion for innovation and improving patient outcomes.
This role is entirely remote, offering the flexibility to work from any approved location. We provide a comprehensive remote onboarding process and ensure our team members have the tools and support needed to excel. Join a forward-thinking company dedicated to making a real difference.
Clinical Research Scientist
Posted 24 days ago
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Job Description
Clinical Research Scientist
Posted 24 days ago
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Job Description
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.
Clinical Research Scientist (Oncology)
Posted 4 days ago
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Job Description
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.
Clinical Research Scientist (Oncology)
Posted 4 days ago
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Job Description
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.
Clinical Research Scientist - Oncology
Posted 8 days ago
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Job Description
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
Posted 8 days ago
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Job Description
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.
Clinical Research Scientist (Oncology)
Posted 12 days ago
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Job Description
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.
Clinical Research Scientist - Oncology
Posted 14 days ago
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Job Description
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.
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.