33 Paediatric Oncology jobs in the United Kingdom

Our client, a renowned institution in Liverpool, Merseyside, UK , is seeking a highly accomplished Senior Medical Researcher specialising in Oncology to contribute to groundbreaking scientific advancements. This hybrid role offers the unique opportunity to conduct innovative research within state-of-the-art facilities while also benefiting from the flexibility of hybrid working arrangements. You will be instrumental in designing and executing complex research projects aimed at understanding cancer biology, developing novel therapeutic strategies, and improving patient outcomes. This position requires a deep commitment to scientific excellence and a passion for making a tangible impact on human health.

Key Responsibilities:

• Lead and conduct independent research projects focused on the molecular mechanisms of cancer, drug resistance, and novel treatment modalities.
• Design, optimise, and perform a variety of laboratory experiments, including cell culture, molecular biology techniques, genomics, proteomics, and in vivo models.
• Analyse and interpret complex experimental data, employing advanced statistical and bioinformatics tools.
• Develop hypotheses, design experiments to test them, and draw robust conclusions.
• Collaborate with a multidisciplinary team of scientists, clinicians, and researchers to advance oncology research.
• Prepare research findings for publication in high-impact peer-reviewed journals and present at national and international conferences.
• Supervise and mentor junior researchers, post-doctoral fellows, and research assistants.
• Manage laboratory resources, including budgets, equipment, and supplies, ensuring efficient operation.
• Ensure strict adherence to laboratory safety protocols, ethical guidelines, and regulatory standards.
• Contribute to the writing of grant proposals to secure funding for new research initiatives.
• Stay current with the latest developments and literature in oncology and related fields.
• Contribute to the strategic direction of the research department.

Qualifications and Skills:

• PhD in Cancer Biology, Molecular Biology, Immunology, Pharmacology, or a closely related field.
• Minimum of 5 years of post-doctoral research experience in oncology, with a strong publication record in reputable journals.
• Extensive hands-on experience with a broad range of molecular and cellular biology techniques relevant to cancer research.
• Proficiency in data analysis software and bioinformatics tools.
• Demonstrated ability to design and execute complex research projects independently.
• Excellent problem-solving skills and critical thinking abilities.
• Strong written and verbal communication skills, with experience in grant writing and manuscript preparation.
• Proven ability to supervise and mentor junior research staff.
• Familiarity with relevant ethical guidelines and regulatory requirements in medical research.
• Ability to work effectively both independently and as part of a collaborative team.
• Experience with animal models of cancer is highly desirable.
• This role requires a commitment to in-person laboratory work and occasional hybrid arrangements.

This is an exceptional opportunity for a dedicated researcher to make significant contributions to cancer research at our Liverpool facility.

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Since AbbVie's inception in 2013, our oncology organization has double in size around the world with a culture of bold innovation, curiosity and determination for patients. We have teams working in over 70 countries which includes oncology-focused R&D and/or manufacturing facilities
Job Description
+ Reporting to the UK Medical Director, leading a team of 26.
+ Based in the offices in Maidenhead (3 days a week) with 2 days flexible working.
+ Highly competitive salary, Car allowance, LTi's, Bonus and comprehensive benefits package.
Overview:
To effectively structure, build and lead the UK Oncology Medical Affairs Department, providing guidance and support to the team in defining critical strategies and executing innovative medical activities that support the therapy area. To inspire and develop a high performing Oncology Medical Affairs team.
To develop strong partnerships with external and internal stakeholders i.e. Healthcare Professionals, members of the Brand Team, Medical Director, Regional and Global Medical Affairs colleagues as well as other internal functions e.g. Site Management and Monitoring, Legal, Finance.
To ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.
Key responsibilities include:
+ Build and provide leadership to the UK Oncology Medical Affairs team
+ Lead the UK Oncology Medical Affairs department in defining critical strategies and executing medical activities that support the therapy area.
+ Ensure proactive scientific and clinical input by members of the Medical Division and the Oncology Medical Affairs Department into the Brand teams and key brand initiatives.
+ Assist and advise Brand team members on promotional activities, and ensure compliance with the ABPI Prescription Medicines Code of Practice
+ Respond to Inter-company Code of Practice complaints and liaise with the PMCPA
+ Develop and maintain in-depth knowledge of the company's products, the therapeutic area and the structure and workings of the NHS
+ Establish and develop strong relationships with key external customers including External Experts, Public Bodies e.g. Department of Health, MHRA and key external influencers e.g. NHSE.
+ Ensure appropriate support by the Medical Affairs Team for relevant personnel on disease/product knowledge
+ Ensure appropriate support to the Site Management and Monitoring team to achieve UK study targets for global clinical trials with UK sites.
+ Ensure clinical support is provided to HTA Department including input into HE strategy and Health Technology Assessment submissions. Also assist with interactions with Market Access/HTA Bodies where appropriate.
+ Ensure clinical support/guidance and training is provided to all other functions within the Medical Division and UK affiliate, as required.
+ Respond to requests for individual named patient supplies as required
+ Ensure appropriate HMT and CME training requirements are met for all physicians within the Medical Affairs Department, for example, support revalidation for doctors with Faculty of Pharmaceutical Medicine.
+ Lead the brand-aligned medical team and ensure its compliance to corporate requirements and processes on medical activities
+ Drive Medical Strategy and align with Global strategies for the Brand within the Brand Team and integrate it into the Brand Plan
+ Oversee Medical activities within the Brand Team, according to local resources and regulations
Qualifications
+ Medically qualified with clinical experience post-registration and GMC registered or PhD scientist or pharmacist background.
+ Experience of leading and developing a team in a complex matrix organisation within the pharmaceutical industry.
+ Experience of working in Oncology would be an advantage.
+ Ability to think and plan strategically and to adopt an open-minded approach to common challenges.
+ Ability to deal with conflicting interests within a multi-functional team and the leadership skills to bring these interests together towards a common goal.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Our client, a leading global pharmaceutical company dedicated to advancing oncology treatments, is seeking an experienced and highly motivated Medical Science Liaison (MSL) to cover the **Nottingham, Nottinghamshire, UK** region. This critical role serves as a vital scientific bridge between the company and key opinion leaders (KOLs) in the medical and scientific community, focusing on the therapeutic area of oncology. You will be responsible for communicating complex scientific and clinical information about our innovative medicines, gathering insights from KOLs, supporting clinical trial activities, and delivering scientific education. The ideal candidate will possess an advanced scientific or clinical degree (MD, PhD, PharmD, or equivalent) with substantial experience in medical affairs, clinical research, or a related scientific discipline within the pharmaceutical industry, specifically in oncology. Exceptional scientific knowledge of cancer biology, treatment modalities, and clinical trial design is essential. Strong communication, presentation, and interpersonal skills are crucial for building and maintaining trusted relationships with KOLs. This field-based role requires extensive travel within the designated territory, as well as occasional travel to conferences and company meetings. The ability to critically evaluate scientific literature, respond to unsolicited medical information requests, and contribute to the development of medical strategies is paramount. We are looking for a passionate advocate for scientific exchange, dedicated to improving patient outcomes through the responsible dissemination of medical and scientific information. If you are a seasoned medical affairs professional with a deep commitment to oncology and a drive for scientific excellence, we encourage you to apply.

Responsibilities:

• Establish and maintain strong, peer-to-peer relationships with oncology Key Opinion Leaders (KOLs) and healthcare professionals.
• Communicate complex scientific and clinical data regarding company products and therapeutic areas.
• Gather insights from KOLs on treatment landscapes, unmet medical needs, and emerging research.
• Provide scientific and clinical education to healthcare providers.
• Support the company's clinical trial efforts, including site identification and investigator engagement.
• Respond accurately and efficiently to unsolicited medical information requests.
• Attend and present at relevant medical congresses and scientific meetings.
• Contribute to the development and execution of the regional medical strategy.
• Collaborate with internal medical, clinical, and commercial teams.
• Ensure compliance with all industry regulations and company policies.

Qualifications:

• Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or clinical discipline.
• Minimum of 3-5 years of experience as a Medical Science Liaison or in a similar medical affairs role within the pharmaceutical industry.
• Specialised expertise and experience in the field of oncology.
• In-depth knowledge of cancer biology, therapeutic strategies, and clinical research.
• Excellent communication, presentation, and interpersonal skills.
• Demonstrated ability to build and maintain relationships with KOLs.
• Strong scientific and clinical data interpretation skills.
• Ability to travel extensively within the assigned territory.
• Understanding of regulatory guidelines and ethical conduct in medical affairs.

Our client, a global biopharmaceutical company dedicated to advancing healthcare, is seeking an accomplished Medical Affairs Manager specializing in Oncology to join their team in **Newcastle upon Tyne, Tyne and Wear, UK**. This strategic role is pivotal in driving medical strategy and engagement within the oncology therapeutic area. You will be responsible for developing and executing comprehensive medical affairs plans, including peer-to-peer scientific exchange with key opinion leaders (KOLs), medical education programs, and support for clinical research initiatives. Your role will involve translating complex scientific data into compelling medical communication strategies, ensuring accurate and compliant dissemination of information. You will serve as a key medical expert, providing scientific and clinical support to internal stakeholders, including marketing, sales, and regulatory affairs. Responsibilities include managing medical advisory boards, evaluating investigator-initiated trial proposals, and contributing to the development of scientific publications. The ideal candidate will possess a Medical Degree (MD), PharmD, or Ph.D. in a relevant life science field, with a minimum of 5 years of experience in medical affairs within the pharmaceutical industry, preferably with a focus on oncology. A deep understanding of oncology, clinical trial design, and regulatory guidelines (e.g., ABPI Code of Practice) is essential. Exceptional communication, presentation, and interpersonal skills are required to build strong relationships with KOLs and internal teams. Strong strategic thinking, project management capabilities, and the ability to work effectively in a cross-functional team environment are critical. This role requires a significant presence on-site for team collaboration, KOL engagement, and operational management. The successful applicant will be a highly motivated and scientifically driven individual committed to advancing patient care through innovative medical affairs strategies.

**Job Overview**
The medical department consists of a Chief Medical Officer, Medical Directors, Sr Medical Directors, Medical Writers, and Safety Associates. The Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or awarded clinical research programs.
The Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. The primary role of Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The principal function of a Medical Monitor is to serve as primary contact for the sponsor medical team and to serve as front line medical resource to support the project team. The Medical Monitor is customarily available 24/7 to answer questions from site coordinators and investigators on protocol inclusion/exclusion criteria, protocol clarifications, and compliance issues, and to provide review of alert labs per sponsor preference. Major duties of the Medical Director are outlined below:
**Essential Functions**
Functions as project team member:
+ Provides medical and scientific input to clinical research programs including review of new business proposals, preclinical and/or clinical data, study protocols, training materials, informed consent, Investigator Drug Brochures, eCRFs, analysis plan designs, clinical study reports, regulatory approval submissions, serious and non-serious adverse event evaluation, and reporting.
+ Ensures medical activities run according to GCP and operate with highest efficiency.
+ Establishes and maintains a network of medical/scientific consultants, etc.
+ Supervises and manages Medical Director activities.
Clinical Activities:
+ Interacts with clients regarding drug development programs, study design and protocol.
+ Reviews and provides input for protocol development. Interacts with key thought leaders and/or sponsor representatives to develop inclusion/exclusion criteria and study endpoints.
+ Interacts in team approach to develop statistical and data management sections of the protocol.
+ Reviews the final protocol for clinical, safety and efficacy variables.
+ Provides project team training on protocol and/or therapeutic areas.
+ Assists team with developing criteria for investigator site selection and networking for potential investigators for study participation. Aids in review and final selection.
+ Participates in subject recruitment and retention activities including individual calls to key opinion leaders, investigators, and site staff and/or participation in teleconference and WebEx presentations.
+ Presents protocol and/or safety reporting information at investigator meetings.
+ Develops project medical monitoring plans as requested.
+ Provides on call coverage for protocol queries and site support.
+ Provides first line contact for investigators and monitors regarding study related medical/safety issues and resolution of study protocol and patient eligibility issues.
Safety Monitoring and SAE Reporting Activities:
+ Verifies the medical accuracy of patient safety data and maintains an ongoing assessment of the safety profile of the study.
+ Provides medical review of SAE reporting, writes and/or reviews SAE narratives, and works with the Safety Management Department to track SAEs and follow-up on outstanding safety queries, interacts with sponsor and discusses safety issues with site as needed.
+ Reviews IND/SUSAR Safety Reports (per sponsor preference), updates to Investigator Brochures, and annual IND reports with sponsor data.
+ In consultation with the sponsor, follow procedures for acquiring knowledge of subject treatment assignments (i.e. breaking the blind).
+ Interact with appropriate FDA officials concerning safety and other study related issues, as requested.
Data Activities:
+ Provides medical review of eCRFs for clinical accuracy.
+ Provides medical review of data analysis plan.
+ Reviews safety fields at case freeze for reconciliation (if needed).
+ Works with data group to reconcile SAE events as needed.
+ Reviews medical coding of adverse events, laboratory data and concomitant medications for accuracy, coherence, consistency, and trends.
+ Reviews data tables, listings, and figures.
+ Reviews and/or writes portions of final clinical study report.
DSMB/Adjudication Committee Activities:
+ May assist sponsor in choosing committee members.
+ May serve as a non-voting member to convene and organize proceedings.
+ May develop operating guidelines in conjunction with committee members and submits these to sponsor for review.
+ May determine data flow with sponsor to ensure reporting accuracy.
+ Can ensure DSMB feedback is given to sites for IRBs.
+ All DSMB activities are usually managed by the IQVIA Biotech Oversight Management Group and not the IQVIA Biotech medical monitor.
Business Development Activities:
+ Work with Business Development to actively solicit new business for Novella Clinical, including assistance with marketing presentations and proposal development.
+ Supports business development activities with proposal development and sales presentations.
+ Participates in feasibility discussions relating to specific project proposals.
Special Projects:
+ Obtain literature searches to acquire background information for study proposals, preparation of training sessions, and interpretation of clinical data, report writing, etc.
+ Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities.
+ Participate in a variety of team quality improvement efforts as necessary.
+ Perform other related duties as assigned or requested by the Chief Medical Officer.
**Qualifications**
+ Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
+ 10 years of experience is required which can include medical practice (hospital/clinic), academia, clinical research, or drug development.
+ 3-5 years of biopharmaceutical (industry) experience is preferred which can be part of the 10-year experience.
+ Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
+ Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
+ Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
+ Excellent oral and written communications skills as well as interpersonal skills are essential.
**Oncology / Hematology**
+ Current or prior license to practice medicine; board certification/eligibility ideal (Preference)
+ Board Certified / Board Eligible: Oncology (Required)
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Our client, a leading global pharmaceutical company specializing in oncology, is seeking an experienced and highly knowledgeable Senior Medical Science Liaison (MSL) to cover the Glasgow, Scotland, UK territory. This critical role involves building and maintaining strong relationships with key opinion leaders (KOLs) in the field of oncology, disseminating scientific and clinical information, and gathering valuable insights to support the company's research and development efforts. The ideal candidate will possess deep scientific expertise in oncology, excellent communication skills, and a proven ability to engage effectively with the medical community.

Key responsibilities of the Senior Medical Science Liaison include:

• Establishing and nurturing strong, peer-to-peer relationships with KOLs, researchers, and healthcare professionals in the oncology therapeutic area.
• Delivering accurate and comprehensive scientific and clinical information regarding company products and relevant disease states.
• Responding to unsolicited requests for medical information from healthcare professionals.
• Gathering and relaying crucial insights from KOLs regarding unmet medical needs, treatment landscapes, and potential research directions.
• Identifying and supporting investigator-initiated research (IIR) opportunities.
• Representing the company at relevant medical conferences, symposia, and advisory boards.
• Providing scientific and clinical training to internal teams as needed.
• Contributing to the development of medical affairs strategies and plans.
• Ensuring compliance with all industry regulations, ethical guidelines, and company policies.
• Staying abreast of the latest scientific advancements, clinical trial data, and treatment guidelines in oncology.

The successful candidate will hold a PhD, PharmD, MD, or equivalent advanced scientific degree, with a minimum of 5 years of experience as an MSL or in a similar medical affairs role within the pharmaceutical industry, preferably in oncology. A strong scientific background in oncology, including deep knowledge of current treatment paradigms and emerging therapies, is essential. Proven ability to build and maintain professional relationships with KOLs is paramount. Excellent presentation, communication, and interpersonal skills are required, along with the ability to articulate complex scientific concepts clearly and concisely. This hybrid role requires regular travel within the assigned territory of Glasgow, Scotland, UK , and occasional national/international travel, with a flexible approach to remote working for administrative tasks. This is an outstanding opportunity to contribute to the advancement of cancer care.

Our client, a leading global pharmaceutical company at the forefront of innovative cancer research, is seeking an exceptional Principal Medical Science Liaison (MSL) to join their rapidly expanding team. This is a fully remote role, offering the opportunity to engage with key opinion leaders (KOLs) and healthcare professionals across the UK. You will be responsible for building and maintaining strong scientific relationships, disseminating complex clinical and scientific information, and gathering valuable insights to support the company's oncology portfolio. This pivotal role requires deep scientific expertise, excellent communication skills, and a strategic approach to medical affairs.

As a Principal MSL, you will serve as a trusted scientific expert, providing in-depth information on investigational and approved products. You will present clinical data, respond to unsolicited medical information requests, and facilitate scientific exchange with KOLs in the field of oncology. Your role will involve understanding the evolving therapeutic landscape, identifying unmet medical needs, and contributing to the strategic development of medical affairs plans. You will gather real-world evidence and competitive intelligence from the field, providing critical feedback to internal medical, R&D, and commercial teams. This position demands a high degree of autonomy and the ability to manage your territory effectively from a remote setting. The ideal candidate will possess a strong scientific background (PhD, PharmD, MD, or equivalent) with extensive experience in medical affairs, clinical development, or medical science liaison roles within the pharmaceutical industry, specifically within oncology.

Key Responsibilities:

• Establish and maintain strong scientific relationships with KOLs and healthcare professionals.
• Disseminate complex clinical and scientific information regarding oncology products.
• Gather insights on treatment patterns, unmet needs, and competitive intelligence.
• Respond to unsolicited medical information requests accurately and scientifically.
• Support clinical trial activities and investigator-initiated studies.
• Contribute to the development and execution of the medical affairs strategy.
• Present scientific data at national and international meetings (as appropriate).
• Collaborate with internal medical, R&D, and commercial colleagues.
• Ensure compliance with all relevant industry codes and regulations.

Qualifications:

• Advanced scientific degree (PhD, PharmD, MD, or equivalent).
• Significant experience as an MSL or in a related medical affairs role.
• Deep understanding of oncology therapeutic areas and clinical practice.
• Exceptional communication, presentation, and interpersonal skills.
• Proven ability to build and maintain relationships with key stakeholders.
• Strong analytical and problem-solving skills.
• Demonstrated understanding of clinical research and drug development processes.
• Ability to work independently and manage a remote territory effectively.
• Excellent knowledge of regulatory guidelines and compliance requirements.

This is a fantastic opportunity for a highly skilled and motivated professional to make a significant impact in the fight against cancer, working remotely in **Bristol, South West England, UK** (or surrounding regions, with travel as needed).

Our client, a prominent global pharmaceutical company, is seeking an experienced Senior Medical Science Liaison (MSL) specializing in Oncology to join their fully remote medical affairs team. In this field-based role, you will serve as a critical scientific and clinical point of contact between the company and key opinion leaders (KOLs), healthcare professionals (HCPs), and research institutions. Your primary responsibility will be to foster scientific exchange, share in-depth clinical and scientific information about our oncology portfolio, and support investigator-initiated studies. This position requires a deep scientific understanding of oncology, excellent communication and interpersonal skills, and the ability to build strong relationships within the medical community, all managed remotely. You will also gather insights from the field to inform clinical development and medical strategy.

Key Responsibilities:

• Establish and maintain strong relationships with KOLs and HCPs in the oncology field.
• Disseminate complex scientific and clinical data regarding our oncology products.
• Respond to unsolicited medical information requests from healthcare professionals.
• Support the development and execution of medical affairs strategies.
• Identify and facilitate opportunities for investigator-initiated research (IIRs).
• Gather and communicate valuable insights from the field regarding treatment landscapes, unmet medical needs, and competitive intelligence.
• Participate in medical conferences, symposia, and other scientific events.
• Collaborate with internal cross-functional teams, including clinical development, regulatory affairs, and marketing.
• Ensure compliance with all industry regulations and company policies.
• Provide scientific training and support to internal stakeholders.
• Contribute to the identification of potential clinical trial investigators.

Qualifications and Experience:

• Advanced degree (Pharm.D., Ph.D., M.D., or equivalent) in a life science, medical, or related field.
• Minimum of 5 years of experience in a Medical Science Liaison or similar medical affairs role within the pharmaceutical industry, with a strong focus on oncology.
• Deep understanding of oncology, including disease mechanisms, treatment paradigms, and clinical trial methodologies.
• Proven ability to build and maintain scientific relationships with KOLs and HCPs.
• Excellent presentation, communication, and interpersonal skills.
• Ability to critically evaluate and interpret complex scientific and clinical data.
• Strong understanding of regulatory and compliance guidelines governing pharmaceutical interactions.
• Demonstrated ability to work independently and manage a territory effectively in a remote setting.
• Proficiency in MS Office Suite and experience with CRM systems for tracking interactions.
• Adaptability and a proactive approach to learning and problem-solving.

This fully remote role offers a highly competitive salary, bonus structure, comprehensive benefits, and the opportunity to make a significant contribution to advancing cancer care.

Our client, a pioneering biotechnology firm at the forefront of medical innovation, is seeking a highly motivated and accomplished Lead Medical Research Scientist specializing in Oncology to join their state-of-the-art research facility in Reading, Berkshire, UK . This is a critical role for an individual with a deep understanding of cancer biology and a passion for translating scientific discoveries into novel therapeutic strategies. You will be responsible for designing, executing, and interpreting complex research projects aimed at identifying and validating new drug targets, as well as developing innovative treatment modalities for various forms of cancer.

Your expertise will be crucial in leading a team of talented researchers, providing scientific direction, and fostering a collaborative and results-driven research environment. This will involve mentoring junior scientists, overseeing experimental design, ensuring data integrity, and staying abreast of the latest advancements in oncology research and drug development. You will also be responsible for securing research grants, writing scientific publications, and presenting findings at international conferences. A significant part of your role will involve close collaboration with cross-functional teams, including clinical development, regulatory affairs, and business development, to ensure seamless progression of projects from bench to bedside.

Key Responsibilities:

• 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.

Qualifications:

• 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.

This is a unique opportunity to make a significant contribution to the fight against cancer in a dynamic and intellectually stimulating environment located in Reading, Berkshire, UK .