6,859 Medical Research jobs in the United Kingdom

• Develop and execute cutting-edge research strategies in oncology.
• Lead and mentor a team of research scientists and technicians.
• Design and conduct in vitro and in vivo experiments.
• Analyze and interpret complex biological data.
• Author high-impact scientific publications and present research findings.
• Collaborate with internal and external stakeholders.
• Manage research budgets and resources effectively.
• Stay current with the latest scientific literature and emerging technologies.

• Ph.D. in Molecular Biology, Cancer Biology, Immunology, or a related field.
• Minimum of 5-7 years of post-doctoral research experience in oncology, with a strong publication record.
• Proven experience in leading research projects and mentoring staff.
• Expertise in cancer cell biology, signaling pathways, and therapeutic development.
• Experience with various molecular and cellular biology techniques.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills.

• Design and execute complex experimental protocols in immunology and related fields.
• Lead independent research projects from conception through to data analysis and publication.
• Develop and validate novel assays and methodologies for studying immune responses.
• Investigate the molecular and cellular mechanisms underlying immune-related diseases.
• Collaborate with a multidisciplinary team of scientists, clinicians, and statisticians.
• Analyse and interpret complex experimental data using appropriate statistical methods.
• Prepare high-quality manuscripts for publication in peer-reviewed journals and present findings at international conferences.
• Mentor and train junior research staff and students.
• Manage laboratory resources, budgets, and procurement for assigned projects.
• Stay current with the latest advancements and literature in immunology and translational medicine.
• Contribute to grant writing and securing external funding for research initiatives.

• Design, execute, and optimize advanced genomic experiments, including Next-Generation Sequencing (NGS) library preparation and data analysis.
• Develop and validate novel genomic assays and protocols for specific research objectives.
• Analyze large-scale genomic datasets using bioinformatics tools and statistical methods.
• Interpret research findings, prepare comprehensive reports, and present results at scientific conferences and internal meetings.
• Supervise and mentor junior research staff, providing technical guidance and training.
• Collaborate with internal and external partners to advance research goals and publish findings in peer-reviewed journals.
• Manage laboratory resources, including equipment maintenance, supply inventory, and budget oversight for research projects.
• Stay current with the latest scientific literature, technological advancements, and best practices in genomics and molecular biology.
• Contribute to grant writing and proposal development to secure funding for new research initiatives.
• Ensure compliance with all laboratory safety protocols, ethical guidelines, and regulatory requirements.

• Ph.D. in Molecular Biology, Genetics, Genomics, Bioinformatics, or a closely related field.
• A minimum of 6 years of post-doctoral research experience in a relevant scientific discipline, with a strong publication record.
• Extensive hands-on experience with various NGS platforms (e.g., Illumina, PacBio) and library preparation techniques.
• Proficiency in bioinformatics tools and programming languages (e.g., R, Python) for genomic data analysis.
• Demonstrated experience in statistical analysis and interpretation of complex biological data.
• Proven ability to lead research projects, mentor junior scientists, and manage laboratory operations.
• Excellent written and verbal communication skills, with the ability to articulate complex scientific concepts effectively.
• Experience in a hybrid work environment, balancing on-site laboratory work with remote data analysis and reporting.
• Strong problem-solving abilities and a rigorous scientific approach.
• Knowledge of CRISPR technology and single-cell genomics is a plus.

This is an exciting opportunity for a medically qualified Clinical Research Fellow to join the Breast Cancer Now programme at King’s College London and contribute to the development of a first-in-human immune priming platform trial in breast cancer. The post holder will be report into Professor Sheeba Irshad and will be based at Guy’s Cancer Centre in London Bridge. 

This post offers hands-on experience in translational trial design, clinical delivery, and immuno-oncology research. The successful applicant will work closely with academic and NHS collaborators including Guy’s and St Thomas’ NHS Trust and the ICR Clinical Trials and Statistics Unit.

The role is ideal for a doctor aiming to undertake or complete a research degree (MD(Res)) and will involve developing trial documentation, contributing to regulatory submissions, and supporting the clinical and translational aspects of the study. The post will focus on intratumoral virotherapy using CRAd657-CD40L, with the goal of converting immune cold breast tumours to immune hot.

This is a full time post (40 Hours per week), and you will be offered an a fixed term contract for 6 months.

Position: Global Healthcare Equity Research Analyst

Location: London

As part of the Global Equity team, you will:

• Conduct deep research and analysis on publicly listed healthcare companies.
• Collaborate and contribute to a high-conviction, sustainability-driven portfolio.
• Travel internationally to meet with companies and gain firsthand insights.
• Play a key role in shaping investment decisions through rigorous valuation and industry analysis.

This is a unique opportunity to build a long-term career in a world-class investment firm that values purpose as much as performance.

They are looking for someone who brings:

• Minimum of 3-4 years of experience covering the healthcare sector in financial services, investment management, or private equity.
• Strong financial modelling and analytical skills.
• Intellectual curiosity and a passion for deep research.
• A clear interest in sustainability and understanding what defines a high-quality, sustainable business.
• Excellent communication skills and a collaborative mindset.
• Confidence, humility, and grit.

If you're ready to make a meaningful impact through sustainable investing, apply here or reach out via email to:

• 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.

• 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.

• 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.

• 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.