What Jobs are available for Medical Research in London?

• Leading the design and development of clinical trial protocols, ensuring scientific rigor and alignment with regulatory requirements.
• Overseeing the statistical planning and analysis of clinical data, working closely with biostatisticians.
• Interpreting complex clinical trial results and providing strategic insights to guide drug development decisions.
• Authoring key study documents, including clinical study reports (CSRs), regulatory submissions (e.g., INDs, NDAs), and manuscripts for peer-reviewed publications.
• Collaborating with cross-functional teams, including regulatory affairs, medical affairs, and project management, to ensure seamless trial execution.
• Providing scientific expertise and leadership throughout the clinical development lifecycle, from Phase I to Phase IV studies.
• Mentoring and guiding junior research scientists and contributing to the scientific advancement of the R&D organisation.
• Staying abreast of the latest scientific advancements, therapeutic trends, and regulatory guidelines within the pharmaceutical industry.
• Presenting research findings at scientific conferences and to internal stakeholders.

• Lead the design and development of clinical trial protocols, ensuring alignment with scientific objectives and regulatory requirements.
• Oversee the planning, execution, and monitoring of Phase I-IV clinical studies.
• Manage and mentor a team of clinical research scientists and associates.
• Collaborate with internal and external stakeholders, including investigators, CROs, and regulatory bodies.
• Analyze and interpret clinical trial data, contributing to scientific publications and presentations.
• Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.
• Develop and maintain strong relationships with key opinion leaders (KOLs) in relevant therapeutic areas.
• Contribute to the strategic direction of the drug development pipeline.
• Prepare clinical study reports and regulatory submission documents.
• Identify and mitigate potential risks and issues in clinical trials.
• Stay abreast of the latest scientific advancements and industry trends.
• Manage project timelines, budgets, and resources effectively.

• PhD or equivalent doctoral degree in a life science, pharmaceutical science, or related discipline.
• Minimum of 8-10 years of experience in clinical research within the pharmaceutical or biotechnology industry.
• Proven experience in leading clinical trial design and execution across multiple phases.
• Extensive knowledge of drug development processes, regulatory affairs (e.g., FDA, EMA), and GCP guidelines.
• Strong understanding of biostatistics and data analysis principles.
• Demonstrated leadership and team management skills.
• Excellent scientific writing, presentation, and communication abilities.
• Proficiency in statistical software packages (e.g., SAS, R) is a plus.
• Ability to work independently and manage multiple complex projects in a remote setting.
• Experience in specific therapeutic areas (e.g., oncology, immunology, CNS) is highly desirable.

• Lead the scientific strategy and design of clinical development programs for assigned therapeutic areas or drug candidates.
• Develop clinical trial protocols, amendments, investigator brochures, and other essential study documents, ensuring scientific accuracy and regulatory compliance.
• Provide scientific expertise and oversight throughout the lifecycle of clinical trials, from initiation to database lock and study report writing.
• Interpret clinical trial data, ensuring robust analysis and accurate reporting of results.
• Collaborate with biostatistics and data management teams to define data analysis plans and review study outputs.
• Serve as a key scientific liaison with regulatory authorities (e.g., MHRA, EMA, FDA) for submissions and inquiries.
• Engage with key opinion leaders (KOLs) and investigators to gather insights, foster collaboration, and ensure optimal trial conduct.
• Stay abreast of the latest scientific advancements, competitive landscape, and regulatory guidelines within the relevant therapeutic areas.
• Mentor and guide junior scientists and contribute to the scientific development of the clinical research department.
• Contribute to the preparation of scientific publications and presentations.
• Participate in the evaluation of new drug targets and development opportunities.

• Advanced scientific degree (Ph.D. or M.D.) in a relevant life science discipline (e.g., Pharmacology, Biology, Medicine).
• Minimum of 7-10 years of progressive experience in clinical research within the pharmaceutical or biotechnology industry.
• Demonstrated expertise in clinical trial design (Phase I-IV), execution, and data interpretation.
• Thorough understanding of ICH-Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Proven ability to lead complex projects and cross-functional teams.
• Excellent scientific writing and oral communication skills, with experience presenting complex data.
• Strong analytical and problem-solving capabilities.
• Experience in specific therapeutic areas such as oncology, immunology, or neurology is highly desirable.
• Ability to work effectively in a hybrid environment, balancing remote and in-office responsibilities in London, England, UK .

• Design and develop clinical trial protocols in accordance with regulatory guidelines and scientific objectives.
• Oversee the execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and other relevant regulations.
• Analyze and interpret clinical trial data, drawing scientifically sound conclusions and contributing to study reports.
• Collaborate with cross-functional teams, including statisticians, data managers, medical writers, and regulatory affairs specialists.
• Prepare regulatory submissions and interact with health authorities.
• Contribute to the selection and evaluation of investigational sites and investigators.
• Provide scientific and technical expertise to support drug development programs.
• Monitor the safety and efficacy of investigational products throughout clinical trials.
• Stay current with scientific literature, emerging technologies, and industry best practices in clinical research.
• Author or contribute to the publication of research findings in peer-reviewed journals and presentations at scientific conferences.
• Mentor junior scientists and contribute to the scientific growth of the team.
• Participate in the development of strategic research plans and pipeline prioritization.

• PhD or PharmD in a relevant scientific discipline (e.g., Pharmacology, Medicine, Biology, Pharmacy).
• Minimum of 8 years of progressive experience in clinical research within the pharmaceutical industry.
• In-depth knowledge of clinical trial design, execution, data analysis, and reporting.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements for drug development.
• Proven track record of successfully leading and contributing to clinical trials.
• Excellent analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication skills, with experience in scientific writing and presentations.
• Ability to collaborate effectively with multidisciplinary teams.
• Experience with statistical analysis and interpretation of clinical data.
• Proficiency in relevant scientific and clinical research software.
• Demonstrated ability to contribute to strategic drug development planning.

• Design and execute complex in-vitro and in-vivo preclinical studies to evaluate novel oncology drug candidates.
• Analyze and interpret experimental data, developing robust conclusions and strategic recommendations for project progression.
• Prepare high-quality scientific reports, manuscripts for publication, and presentations for internal and external stakeholders.
• Contribute to the development of regulatory submission documents (e.g., IND, NDA).
• Collaborate effectively with cross-functional teams, including discovery biology, translational medicine, and clinical development.
• Mentor junior scientists and contribute to a positive and innovative research environment.
• Stay abreast of the latest advancements in oncology research, therapeutic modalities, and drug development technologies.
• Ensure all research activities comply with relevant ethical guidelines and regulatory standards.
• Manage external collaborations with academic institutions and contract research organizations (CROs).
• Contribute to the strategic direction of the oncology pipeline.

• Ph.D. in Oncology, Molecular Biology, Pharmacology, or a related life science discipline.
• Minimum of 5 years of post-doctoral or industry experience in cancer research, with a strong track record of scientific achievement.
• Proven expertise in preclinical oncology drug discovery and development, including a deep understanding of cancer biology, immunology, and targeted therapies.
• Proficiency in a range of laboratory techniques relevant to oncology research (e.g., cell culture, molecular biology assays, flow cytometry, western blotting, IHC, animal models).
• Excellent data analysis and interpretation skills, with experience using relevant statistical software.
• Strong written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
• Demonstrated ability to work independently and as part of a collaborative team in a remote setting.
• Experience in project management and leading research initiatives is highly desirable.
• Familiarity with regulatory requirements for drug development.

• Contribute to the design and development of innovative clinical trial protocols for oncology indications, ensuring scientific rigor and compliance with regulatory requirements.
• Oversee the execution of clinical studies, from site selection and initiation through to study close-out.
• Analyse and interpret complex clinical data, including safety, efficacy, and biomarker data.
• Prepare and present study results for internal stakeholders, regulatory submissions, and scientific publications.
• Collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, R&D, and external investigators.
• Provide scientific and clinical expertise to guide the progression of drug candidates through the development pipeline.
• Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and other relevant regulations.
• Contribute to the development of scientific strategy and research plans for the oncology portfolio.
• Mentor and guide junior research scientists and clinical trial staff.
• Review and critically evaluate scientific literature relevant to oncology drug development.
• Participate in scientific conferences and represent the company's research efforts.
• Manage relationships with key opinion leaders (KOLs) and external research partners.

• PhD or MD in a relevant scientific discipline (e.g., Oncology, Immunology, Molecular Biology, Pharmacology).
• Minimum of 6 years of experience in clinical research, with a significant focus on oncology drug development.
• In-depth knowledge of oncology therapeutic areas, disease mechanisms, and current treatment landscapes.
• Proven experience in clinical trial design, execution, and data analysis.
• Strong understanding of GCP, regulatory requirements, and drug development processes.
• Excellent scientific writing and communication skills, with a track record of publications.
• Demonstrated ability to work collaboratively in a multidisciplinary, hybrid team environment.
• Strong analytical and problem-solving skills.
• Proficiency in data analysis software and statistical methods.
• Ability to manage multiple projects and deadlines effectively.

Quantinuum is looking for the next scientist to join the Quantum Error Correction (QEC) team in the United Kingdom. If selected, you will contribute to the architectural design and implementation of our QEC stack. This includes projects from the more abstract discovery of QEC codes with good properties and their universal fault-tolerant (FT) gate sets, passing through the big-picture simulation, distribution and estimation of quantum resources in our future generations of quantum devices, to the more practical design, compilation and decoding of FT or partially-FT QEC primitives and complete algorithms in our existing trapped-ion quantum computers.

Based in the London-Victoria or Cambridge offices, you will be working in a research-focused group with scientific direction from experienced QEC researchers, with a close connection to hardware and software engineers. You will produce research papers and software libraries, with freedom to think independently and creatively, making it an excellent opportunity to advance the theory and practice of quantum computing while developing your professional and academic career.

• Researching QEC methods and FT algorithms to run on real and simulated quantum computers.
• Collaborating with hardware and software engineers to implement existing and new techniques.
• Writing articles and publishing in leading scientific journals.
• Developing software libraries that accelerate the research in QEC.
• Keeping up-to-date with the literature of the field.
• Participate in the day-to-day activities of the QEC team: discussions, journal club, seminars…

• A Ph.D. degree or equivalent – or will have submitted their thesis prior to taking up the position – in Maths, Computer Science, Physics or a related discipline.
• A strong research record showing evidence of your ability to understand the fundamentals of QEC and contribute towards new ideas.
• Communicating scientific ideas clearly and precisely, both verbally and in writing.

• Scientific computing, programming in Python, and preferably one or more of high-speed languages like C++, Rust, Julia.

What is in it for you?

Working alongside a highly talented team, with leading names in the quantum computing industry. We offer a highly competitive package, equity, 28 days of paid holiday (in addition to public holidays), a workplace pension, a positive approach to flexible working and enhanced parental and adoption benefits.

About Us:

Quantinuum is the world's largest integrated quantum company, driving breakthroughs in materials discovery, cybersecurity, and next-generation quantum AI. With a team of more than 600 employees, including more than 420 of them being scientists and engineers, we are leading the worldwide quantum computing revolution.

By uniting best-in-class software with high-fidelity hardware, our integrated full-stack approach is accelerating the path to practical quantum computing and scaling its impact across multiple industries.

As we celebrate the International Year of Quantum, there has never been a more exciting time to be part of this rapidly evolving field. By joining Quantinuum, you'll be at the forefront of this transformative revolution, shaping the future of quantum computing, pushing the limits of technology, and making the impossible possible.

Visit our news pages to learn more about Quantinuum and our scientific breakthroughs and achievements:

Quantinuum Intro Video: The Future of Quantum Computing

Please note that employment with us is subject to successfully passing our pre-employment screening checks. We are an inclusive equal opportunity employer. You will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

• Conducting original research in Artificial Intelligence and related fields.
• Developing and implementing novel AI algorithms and models.
• Designing and executing experiments to test hypotheses and validate research findings.
• Analysing large datasets and extracting meaningful insights using advanced statistical methods.
• Collaborating with other researchers and engineers to develop proofs-of-concept and prototypes.
• Contributing to academic publications, conference presentations, and patent applications.
• Staying abreast of the latest advancements and trends in AI research and development.
• Evaluating and integrating new AI technologies and methodologies.
• Mentoring junior researchers and interns.
• Presenting research findings to both technical and non-technical audiences.

• Ph.D. in Computer Science, Artificial Intelligence, Machine Learning, or a closely related discipline.
• Proven track record of research excellence, demonstrated through publications in top-tier AI conferences and journals.
• Strong theoretical and practical knowledge of machine learning, deep learning, and related areas.
• Proficiency in programming languages commonly used in AI research (e.g., Python, C++).
• Experience with deep learning frameworks such as TensorFlow, PyTorch, or Keras.
• Familiarity with relevant AI libraries and tools.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong communication and collaboration abilities, essential for a hybrid team environment.
• Ability to work independently and manage research projects effectively.
• Passion for AI and a drive to contribute to significant advancements in the field.