73 Clinical Oncology jobs in the United Kingdom

**Role: Clinical Research Associate (12+ months' monitoring and Oncology experience required)**
**Location: Must be based in the UK, nationwide travel**
**Fully sponsor dedicated**
As a CRA you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
As Clinical Research Associate, you will be dedicated to one of our global enterprises who are focused on healthcare and agriculture. It develops and markets pharmaceuticals, consumer health products, crop protection solutions, seeds, and digital farming technologies
**Your responsibilities include, but are not limited to: Allocation, initiation and conduct of trials:**
+ Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. Is the frontline liaison between ICON and sites to ensure successful collaboration, meeting ICON expectation on milestone and deliveries
+ Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and our clients procedures. Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate.
+ Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions
+ Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.). Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. Attends onboarding-, disease indication and project specific training and general CRA training as required
+ Documents monitoring activities appropriately following ICON standards. Collaborates with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans,as needed. Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines.
+ Performs additional task as assigned Delivery of quality data and compliance to quality standards
+ Monitors studies as per current legislations, ICH/GCP and our clients standards. Ensures timely delivery, of high quality, robust and reliable data of the monitored sites to support the goals of Trial Monitoring as defined by Trial Monitoring. (ADIS, DBL). Identifies issues at sites; resolves issues and escalate as appropriate
+ Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry. Ensures the site Investigator Folder is up to date. Is responsible for collecting essential documents from site and accountable to keep sTMF(s) current. Supports the implementation of innovative processes and technologies Budget and productivity
+ Negotiates investigator remuneration; prepares financial contracts between ICON and investigational sites and investigators. Ensures that payments are appropriately triggered to investigational sites.
**You must have the following:**
- Right to work in the UK
- Up to 2 years pharmaceutical/CRO industry experience
- Good knowledge of drug development process specifically clinical trial/research
- Knowledge of international standards (GCP/ICH, FDA, EMEA)
- 12+ months' monitoring experience required
**Important for the role:**
- Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.
- A minimum of 50% overnight travel may be required.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs
+ Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
+ Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Our client is seeking a meticulous and organized Clinical Research Coordinator to support critical oncology research studies in **Southampton, Hampshire, UK**. This role is fundamental to the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. You will be responsible for a range of activities, including patient recruitment and screening, informed consent process, data collection and entry, and study documentation management. This involves working closely with principal investigators, research nurses, and study sponsors to facilitate the smooth progression of clinical trials. Key duties include scheduling patient visits, managing study supplies, and ensuring accurate and timely completion of case report forms (CRFs) and other study-related documents. You will also play a vital role in monitoring patient compliance and safety, reporting any adverse events promptly. The ideal candidate will have a strong understanding of clinical trial processes, GCP (Good Clinical Practice) guidelines, and regulatory requirements. Excellent organizational skills, meticulous attention to detail, and proficiency in data management software are essential. Strong interpersonal and communication skills are required to interact effectively with patients, healthcare professionals, and study teams. Previous experience in clinical research, particularly in oncology, is highly desirable. A background in nursing, life sciences, or a related field would be beneficial. Join our client to contribute to advancing cancer treatments through impactful research.

Key Responsibilities:

• Coordinate the conduct of clinical trials according to study protocols and GCP guidelines.
• Screen potential participants for eligibility and manage the informed consent process.
• Schedule patient appointments and manage study-related visits.
• Collect, manage, and accurately enter clinical data into study databases.
• Maintain all study-related documentation and regulatory files.
• Monitor patient adherence to the study protocol and report any deviations.
• Record and report adverse events and serious adverse events promptly.
• Liaise with investigators, research staff, and study sponsors.
• Manage study supplies and equipment.
• Ensure compliance with all applicable regulatory requirements.

Required Qualifications:

• Bachelor's degree in Nursing, Life Sciences, or a related field.
• Proven experience as a Clinical Research Coordinator or in a similar role.
• Thorough understanding of clinical trial phases, GCP, and regulatory requirements.
• Excellent organizational and time management skills.
• Meticulous attention to detail in data collection and documentation.
• Strong interpersonal and communication skills, with the ability to interact with patients and professionals.
• Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Ability to work independently and as part of a multidisciplinary team.
• Knowledge of oncology clinical research is a significant advantage.

Our client, a leading pharmaceutical company, is seeking a highly motivated Clinical Research Scientist to join their innovative oncology team based in London, England, UK . This role is critical in advancing groundbreaking cancer therapies from preclinical development through to clinical trials and regulatory approval. The successful candidate will be instrumental in designing, implementing, and managing clinical studies, ensuring adherence to Good Clinical Practice (GCP) and relevant regulatory guidelines. Responsibilities include developing study protocols, managing investigator sites, overseeing data collection and analysis, and preparing regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, R&D, regulatory affairs, and marketing, to ensure the successful execution of clinical programs. A key aspect of this role involves staying at the forefront of scientific advancements in oncology, identifying new research opportunities, and contributing to the strategic direction of the company's drug development pipeline. The ideal candidate will possess a PhD or equivalent in a relevant scientific discipline (e.g., oncology, pharmacology, molecular biology) and have a minimum of 3-5 years of experience in clinical research within the pharmaceutical industry, specifically with oncology trials. Strong understanding of drug development processes, clinical trial methodologies, and regulatory requirements (e.g., FDA, EMA) is essential. Excellent analytical, problem-solving, and project management skills are required, along with outstanding written and verbal communication abilities. This position offers a competitive salary, comprehensive benefits package, and the opportunity to make a significant impact on the lives of cancer patients worldwide within a supportive and collaborative work environment.

Key Responsibilities:

• Design and develop clinical trial protocols for oncology studies.
• Oversee the execution of clinical trials, ensuring compliance with GCP and regulatory standards.
• Manage relationships with clinical trial sites, investigators, and study personnel.
• Monitor study progress, data quality, and patient safety.
• Analyze clinical trial data and prepare study reports and publications.
• Contribute to regulatory submissions (e.g., IND, NDA).
• Collaborate with cross-functional teams to achieve project goals.

Qualifications:

• PhD or equivalent in Oncology, Pharmacology, or a related life science field.
• 3-5 years of experience in clinical research in the pharmaceutical industry, with a focus on oncology.
• Thorough knowledge of clinical trial design, conduct, and data analysis.
• Familiarity with GCP and relevant regulatory guidelines.
• Excellent scientific and medical writing skills.
• Strong project management and organizational abilities.
• Ability to work effectively in a team environment.

Our client, a prominent pharmaceutical company committed to advancing healthcare solutions, is seeking a dedicated Clinical Research Associate (CRA) to support their groundbreaking oncology research programs. This role is site-based and requires regular travel to clinical trial sites across the South West region, with a primary focus on the Plymouth, Devon, UK area. As a CRA, you will be responsible for monitoring clinical trial conduct, ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your duties will include site initiation, routine monitoring visits (on-site and remote), site evaluation, and ensuring accurate and timely data collection and reporting. You will act as the primary liaison between the study sites and the sponsor, addressing any issues that arise during the trial and providing necessary support to investigators and site staff. The ideal candidate will have a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field, along with a minimum of 2-3 years of experience as a CRA, preferably within oncology. Strong knowledge of GCP, ICH guidelines, and regulatory affairs is essential. Excellent organizational, communication, and interpersonal skills are crucial for building effective relationships with clinical sites. You must possess a valid UK driver's license and be comfortable with extensive travel. A meticulous approach to detail and the ability to manage multiple priorities effectively are key. This is a fantastic opportunity to contribute to vital cancer research, work within a highly respected pharmaceutical organization, and develop your career in clinical research. If you are a passionate and experienced CRA looking for a challenging site-based role, we encourage you to apply.

Our client, a pioneering pharmaceutical company at the forefront of developing life-saving cancer therapies, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their dynamic team in Cardiff, Wales, UK . This hybrid role offers a blend of essential site monitoring and remote-based administrative tasks, allowing for a balanced approach to clinical trial management. You will be instrumental in ensuring the quality, integrity, and compliance of clinical trials in line with Good Clinical Practice (GCP) guidelines and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits to clinical trial sites. You will assess the progress of clinical projects, ensure data accuracy and completeness, and manage investigational product. Building and maintaining strong relationships with investigators, site staff, and internal project teams is crucial. The ideal candidate will have a thorough understanding of clinical trial processes, regulatory affairs, and data management. Excellent communication, organisational, and problem-solving skills are essential. You must be adept at managing multiple priorities and working effectively in a fast-paced environment. A proactive approach to identifying and resolving issues, as well as a commitment to patient safety and data integrity, are paramount. This role requires a degree in a life science or related field and demonstrable experience as a CRA. Travel to clinical sites will be required as part of the hybrid working model. This is an exceptional opportunity to contribute to cutting-edge research and make a significant impact on the lives of patients undergoing cancer treatment.
Responsibilities:

• Conduct site selection, initiation, monitoring, and close-out visits for clinical trials.
• Ensure compliance with study protocols, GCP, and regulatory requirements.
• Verify accuracy and completeness of clinical data by reviewing source documents.
• Manage investigational product and study supplies at trial sites.
• Build and maintain strong relationships with investigators and site personnel.
• Identify, track, and resolve site-level issues.
• Prepare and present clinical study progress reports.
• Ensure timely submission of essential documents.
• Collaborate with internal teams, including data management and regulatory affairs.
• Contribute to protocol development and site feasibility assessments.

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Proven experience as a Clinical Research Associate (CRA).
• In-depth knowledge of GCP, ICH guidelines, and clinical trial processes.
• Strong understanding of oncology therapeutic areas.
• Excellent monitoring and auditing skills.
• Exceptional organisational, communication, and interpersonal skills.
• Ability to travel to clinical sites as required.
• Proficiency in clinical trial management systems (CTMS) and EDC.
• Strong problem-solving and decision-making abilities.

Our client, a pioneering biopharmaceutical company focused on innovative cancer therapies, is seeking a highly motivated and experienced Clinical Research Scientist to join their expanding global team. This is a fully remote position, offering the flexibility to work from anywhere within the UK. You will play a critical role in the design, execution, and analysis of clinical trials for novel oncology treatments. Your responsibilities will include developing clinical trial protocols, identifying and qualifying clinical sites, managing trial budgets, and overseeing the ethical conduct of studies in compliance with GCP and regulatory guidelines. You will collaborate closely with internal and external stakeholders, including principal investigators, clinical research associates, statisticians, and regulatory affairs specialists, to ensure the successful progression of clinical development programs. Data analysis and interpretation, authoring clinical study reports, and contributing to regulatory submissions (e.g., INDs, NDAs) will be integral to your role. The ideal candidate will possess a PhD or Master's degree in a life science, medical, or related field, coupled with significant experience in clinical research within the pharmaceutical or biotech industry, with a strong emphasis on oncology. A deep understanding of drug development processes, clinical trial methodology, and regulatory requirements is essential. Exceptional analytical, problem-solving, and critical thinking skills are required, along with the ability to manage multiple projects simultaneously in a fast-paced, remote environment. Strong written and verbal communication skills are crucial for effective collaboration and reporting. Experience with common CTMS, EDC systems, and statistical software packages is highly advantageous. This is an exceptional opportunity to contribute to groundbreaking research and make a tangible impact on the lives of cancer patients worldwide, while enjoying the benefits of a remote-first working culture.

Our client, a leading pharmaceutical company, is seeking an experienced Clinical Research Associate (CRA) to support their oncology clinical trials, operating on a hybrid model with travel to sites near Manchester . This pivotal role involves ensuring the effective management and monitoring of clinical trials to meet regulatory requirements and project milestones. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and experience in site selection, initiation, monitoring, and close-out activities. Responsibilities include verifying the accuracy and completeness of clinical data, ensuring subject safety and rights are protected, managing investigational product accountability, and troubleshooting issues at study sites. You will be responsible for conducting routine site visits, assessing protocol adherence, and communicating effectively with investigators and site staff. A Bachelor's degree in a life science or related field is required, along with proven experience as a CRA. Excellent organizational, communication, and analytical skills are essential. The ability to travel to clinical sites on a regular basis is a must. If you are a dedicated and meticulous professional with a passion for clinical research and a desire to contribute to the development of life-saving cancer therapies, this is an excellent opportunity to join our dedicated team.

Our client, a leading pharmaceutical innovator, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their expanding team in Norwich, Norfolk, UK . This is a fantastic opportunity to contribute to cutting-edge drug development within the oncology sector, working on pivotal clinical trials that have the potential to transform patient lives. The CRA will be responsible for the full-cycle monitoring of clinical trials, ensuring compliance with Good Clinical Practice (GCP), protocols, and regulatory requirements. Key duties include site selection, initiation, monitoring, and close-out visits, as well as managing data verification and query resolution. You will serve as the primary liaison between the sponsor and study sites, building strong relationships with investigators and site staff to ensure efficient trial conduct and high-quality data collection. The role demands excellent organizational skills, a thorough understanding of clinical trial processes, and the ability to travel regularly to clinical sites. You must be proficient in electronic data capture (EDC) systems and have a solid grasp of medical terminology, particularly in oncology. This position offers a chance to work with a dynamic team of professionals and play a crucial part in bringing life-saving treatments to market. Responsibilities include:

• Conducting site visits (qualification, initiation, interim monitoring, close-out).
• Ensuring adherence to study protocols, SOPs, and regulatory guidelines.
• Monitoring patient recruitment and retention.
• Verifying data accuracy and completeness through source data verification (SDV).
• Resolving data queries in a timely manner.
• Training and supporting site staff on study procedures.
• Managing investigational product accountability.
• Preparing and presenting monitoring visit reports.
• Ensuring regulatory compliance and maintaining trial documentation.

Qualifications required:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Previous experience as a CRA or in a similar clinical research role.
• In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
• Strong understanding of oncology.
• Excellent communication, interpersonal, and presentation skills.
• Proficiency in EDC systems and clinical trial management software.
• Willingness to travel extensively.

Our client, a leading pharmaceutical innovator, is searching for a dedicated and experienced Clinical Research Scientist to join their cutting-edge research division. This fully remote position offers the chance to contribute significantly to the development of novel therapies within the oncology field. You will be instrumental in designing, executing, and analyzing clinical trials, ensuring adherence to regulatory guidelines and best practices. Responsibilities include developing study protocols, selecting investigational sites, and collaborating with Principal Investigators and site staff. A critical part of your role will involve data analysis and interpretation, drawing conclusions from complex datasets to inform drug development strategies. You will also prepare clinical study reports, regulatory submissions, and scientific publications. This role demands a strong understanding of pharmaceutical drug development processes, regulatory affairs, and clinical trial management. The ideal candidate will possess excellent communication, problem-solving, and project management skills, enabling effective collaboration with cross-functional teams globally. You must be comfortable working independently and managing your workload effectively in a remote setting. This is an exceptional opportunity to make a tangible impact on patient lives and advance the fight against cancer, all while working remotely to support our client's mission, originating from **Leicester, Leicestershire, UK**. If you are a passionate scientist with a drive for innovation in oncology drug development, we want to hear from you.