53 Clinical Oncology jobs in the United Kingdom

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.

A leading pharmaceutical company with a significant presence in **Coventry, West Midlands, UK**, is seeking a highly skilled Clinical Research Scientist specializing in Oncology. This pivotal role involves contributing to the development of innovative cancer therapies, from early-stage research through to clinical trials. The successful candidate will be instrumental in designing, implementing, and analyzing complex research studies, ensuring compliance with regulatory standards and ethical guidelines.

Key responsibilities include developing research protocols, identifying and assessing suitable clinical trial sites, and managing relationships with investigators and study personnel. You will be involved in data collection, analysis, and interpretation, preparing comprehensive study reports, and presenting findings to internal and external stakeholders. This role requires a deep understanding of cancer biology, therapeutic targets, and the drug development process. You will collaborate closely with cross-functional teams, including regulatory affairs, biostatistics, and medical affairs, to ensure the successful execution of clinical programs.

The ideal candidate will hold a PhD or Master's degree in a relevant life science discipline (e.g., Pharmacology, Molecular Biology, Biochemistry, or a related field) and possess a minimum of 3-5 years of experience in clinical research, preferably within the oncology therapeutic area. Proven experience in clinical trial management, data analysis software (e.g., SAS, R), and strong knowledge of ICH-GCP guidelines are essential. Excellent written and verbal communication skills are required, along with the ability to work independently and as part of a team in a fast-paced environment. This position offers the opportunity to make a significant impact on the lives of cancer patients by advancing cutting-edge treatments. Join a company committed to scientific excellence and patient well-being.

Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is seeking a highly skilled and dedicated Clinical Research Associate (CRA) to support their vital oncology clinical trials. This is a fully remote position, allowing you to contribute to life-changing research from anywhere within the UK. As a CRA, you will be responsible for monitoring clinical trial sites, ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Your role will involve site initiation, routine monitoring visits, close-out activities, and the verification of data accuracy and integrity. You will play a crucial part in the drug development process, working closely with investigators, study coordinators, and internal teams to ensure patient safety and data quality. The ideal candidate will have a strong background in clinical research, with specific experience in oncology trials. Excellent knowledge of GCP, regulatory affairs, and clinical trial processes is essential. You must possess exceptional organizational skills, meticulous attention to detail, and the ability to manage multiple priorities effectively in a remote setting. Strong interpersonal and communication skills are vital for building rapport with site staff and fostering collaborative relationships. This role offers the opportunity to work on cutting-edge therapies and make a tangible difference in the lives of patients battling cancer. If you are a motivated and experienced CRA passionate about advancing oncology research and seeking a rewarding, fully remote career opportunity, we encourage you to apply.
Key Responsibilities:

• Conduct site initiation, monitoring, and close-out visits.
• Ensure compliance with study protocols, SOPs, and regulatory guidelines (GCP, ICH).
• Verify the accuracy, completeness, and consistency of clinical data.
• Monitor patient safety and report adverse events promptly.
• Manage study site operations and resolve site-level issues.
• Build and maintain strong relationships with investigative site staff.
• Prepare monitoring reports and communicate findings to project teams.
• Ensure timely submission of essential documents.
• Contribute to the development of study-related documents.

Qualifications:

• Proven experience as a Clinical Research Associate, preferably in oncology.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Experience with clinical trial site management and monitoring.
• Excellent understanding of clinical trial processes and documentation.
• Strong analytical, organizational, and time-management skills.
• Exceptional communication and interpersonal abilities.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Bachelor's degree in a life science, nursing, or a related healthcare field.

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
The Medical Director of Hematology/Oncology provides medical monitoring to multiple clinical trials. Additionally, the Medical Director guides the project teams to design and implement clinical studies at high quality and in a time and cost-effective manner in line with the department and corporate goals and within regulatory and resource guidelines.
**Responsibilities**
+ Provide medical monitoring to multiple hematology/oncology clinical trials
+ Lead project/study teams to design and implement hematology/oncology clinical studies
+ Write protocols, investigator brochures, clinical study reports and review clinical trial documents
+ Conduct investigator meetings and lead site initiation visits with clinical trial investigators
+ Implement and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets
+ Translate findings from research and nonclinical studies into clinical development opportunities
+ Interact with clinical investigators and thought leaders
+ Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines
+ Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner.
+ Work in a cross-functional team environment, including with clinical operations, biomarker specialists, CROs, and regulatory affairs
+ Provide clinical expertise and input for regulatory filings (i.e., BLA, MAA) as well as response to questions from regulatory authorities in the context of IND submissions, clinical trial applications or filing procedures
+ Provide clinical guidance and work in a team environment in interactions with external stakeholders (medical experts, advisory boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory, Medical Affairs, and Commercial)
**Requirements:**
+ MD/DO degree and clinical development experience in the pharmaceutical industry.
+ Board certification/specialization in Hematology or Oncology and experience managing oncology trials.
+ CAR-T therapeutic area experience (preferred)
+ Multiple myeloma disease area expertise (required)
+ Phase 2 or 3 study experience within the pharmaceutical industry.
+ Relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience.
+ Demonstrated clinical development strategist with experience designing, implementing, and conducting clinical trials, with emphasis on late-stage clinical development.
+ Knowledge of carrying out hematology/oncology clinical trials, including knowledge of hematology/oncology treatment options
+ Strategic leadership and tactical skills, excellent initiative, and judgment
+ Demonstrated ability to develop and maintain excellent working relationships with both internal colleagues and external contacts, including key thought leaders, and investigators
+ Demonstrated ability to work well in teams in a cross functional manner
+ Ability to communicate and work in a self-guided manner with scientific/technical personnel
+ Ability to think critically, and demonstrated troubleshooting and problem-solving skills
+ Self-motivated and willing to accept temporary responsibilities outside of initial job description
+ Comfortable in a dynamic small company environment with minimal direction and able to adjust workload based upon changing priorities
+ May travel up to 25%
+ Must be based in Stockley Park Gilead Office
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.

We are seeking an experienced and highly motivated Senior Clinical Research Associate (CRA) to join our innovative pharmaceutical team based in Oxford, Oxfordshire, UK . This pivotal role involves overseeing and managing clinical trials from initiation to close-out, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements.

Key Responsibilities:

• Plan, initiate, monitor, and close-out clinical trial sites.
• Ensure data integrity and accuracy by conducting source data verification and reviewing case report forms (CRFs).
• Manage relationships with investigators, site staff, and other stakeholders.
• Train and mentor junior CRAs.
• Prepare for and participate in regulatory authority inspections.
• Contribute to the development of study protocols and other essential documents.
• Manage site budgets and timelines effectively.
• Identify and report adverse events and protocol deviations promptly.
• Ensure compliance with all applicable regulations and company policies.
• Travel to sites for monitoring visits (pre-study, initiation, routine, and close-out).

Qualifications:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree or PhD is preferred.
• Minimum of 5 years of experience as a CRA in the pharmaceutical industry, with a strong focus on oncology trials.
• In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
• Excellent understanding of clinical trial processes and documentation.
• Proven ability to manage multiple sites and projects simultaneously.
• Strong communication, interpersonal, and organizational skills.
• Proficiency in medical terminology and clinical research databases.
• Ability to travel up to 60% of the time, with a valid driver's license.
• Experience with electronic data capture (EDC) systems is essential.

This is an exciting opportunity to contribute to cutting-edge research in a dynamic and supportive environment. If you are a meticulous and driven CRA looking to advance your career, we encourage you to apply.

Our client, a leading pharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to support their oncology clinical trial programs. This role offers a hybrid working model, requiring a balance of remote work for administrative tasks and monitoring, with essential on-site visits to clinical trial sites. You will be responsible for overseeing the conduct of clinical trials, ensuring compliance with study protocols, GCP guidelines, and regulatory requirements. Key responsibilities include site selection and initiation, monitoring site performance, data verification, and ensuring patient safety. The ideal candidate will have a degree in a life science or related field, with significant experience as a CRA, particularly in oncology trials. A strong understanding of ICH-GCP guidelines, regulatory affairs, and clinical trial management processes is essential. You should possess excellent organizational skills, attention to detail, and the ability to manage multiple priorities effectively. Strong communication and interpersonal skills are crucial for building and maintaining relationships with investigators, site staff, and internal project teams. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. You must be a self-starter, capable of working independently with minimal supervision, and committed to meeting project timelines and objectives. The hybrid nature of this role allows for efficient remote data review and communication, complemented by critical on-site monitoring to ensure the integrity and quality of trial data. We are dedicated to advancing cancer research and patient care, and this role is integral to our mission. Join a passionate team driving innovation in pharmaceutical development and contributing to life-saving treatments. Your expertise will be vital in ensuring the successful execution of our clinical research initiatives. The role is based in the Birmingham, West Midlands, UK area, blending remote responsibilities with necessary site engagement.

Our client, a leading biopharmaceutical company, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dynamic team in **Portsmouth, Hampshire, UK**. This is an exciting opportunity to contribute to groundbreaking oncology research and drug development. The Senior CRA will be responsible for monitoring clinical trials, ensuring compliance with protocols and regulatory requirements, and managing relationships with investigational sites. Key responsibilities include site selection and initiation, patient recruitment, data collection and management, and site closure. You will also be involved in developing study plans, managing budgets, and identifying and mitigating risks. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory affairs within the pharmaceutical industry. You will need to demonstrate excellent organizational skills, meticulous attention to detail, and the ability to work independently and as part of a multidisciplinary team. This role requires strong communication and interpersonal skills to effectively liaise with investigators, study coordinators, and internal stakeholders. Travel to sites will be required, balanced with flexibility for remote work. A Bachelor's degree in a life science or healthcare-related field is essential, along with a minimum of 5 years of direct CRA experience. Proven experience in oncology trials is highly preferred. The ability to analyze and interpret clinical data, identify trends, and implement corrective actions is crucial. This position offers a competitive salary, comprehensive benefits package, and opportunities for professional development and career advancement within a globally recognized organization. Join us and make a significant impact on the future of cancer treatment. If you are a motivated and detail-oriented CRA looking for a challenging and rewarding role, we encourage you to apply.

Our client is seeking a meticulous and experienced Remote Clinical Data Manager to play a vital role in their oncology research programs. This fully remote position allows you to contribute significantly to groundbreaking clinical trials from the comfort of your own home, with a primary focus on the **Nottingham, Nottinghamshire, UK** region's patient data but managed globally. You will be responsible for the end-to-end management of clinical trial data, ensuring its accuracy, completeness, and compliance with regulatory standards (e.g., ICH-GCP, FDA). Key responsibilities include developing data management plans, designing electronic data capture (EDC) systems, setting up edit checks, managing data review processes, and overseeing database lock.

The ideal candidate will possess a Bachelor's or Master's degree in a relevant life science or health-related field, coupled with a minimum of 3-5 years of progressive experience in clinical data management within the pharmaceutical or biotechnology industry, specifically in oncology. Proficiency with EDC systems (e.g., Medidata Rave, Oracle Clinical) and a strong understanding of clinical trial processes are essential. You must be highly organised, detail-oriented, and capable of managing multiple projects simultaneously in a remote setting. Excellent communication skills are required to liaise effectively with internal teams (clinical operations, biostatistics, programming) and external vendors. This role demands a proactive approach to problem-solving and a commitment to maintaining data integrity and patient confidentiality. You will be instrumental in ensuring the successful execution of clinical trials by providing high-quality data that supports critical decision-making.

Our client, a leading pharmaceutical company, is looking for an experienced Senior Clinical Research Associate (CRA) to join their expanding team. This is a fully remote position, offering the flexibility to work from anywhere in the UK, with travel to sites as required. You will play a crucial role in managing and overseeing clinical trials, ensuring they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits, as well as ensuring data accuracy and patient safety. You will serve as the primary point of contact for study sites, fostering strong relationships with investigators and site staff. The ideal candidate will have extensive experience as a CRA, specifically within oncology trials, and a deep understanding of GCP, ICH guidelines, and regulatory submission processes. Strong organizational, communication, and problem-solving skills are essential. We are seeking a highly motivated, detail-oriented individual who can manage multiple projects, drive trial progress, and ensure the highest standards of clinical trial conduct. Your ability to work independently and effectively manage relationships with sites will be key to success in this remote role.

Responsibilities:

• Conduct site feasibility, selection, initiation, monitoring, and close-out visits.
• Ensure clinical trials are conducted in compliance with GCP, ICH guidelines, and all applicable regulations.
• Oversee data management and ensure the accuracy and completeness of trial data.
• Manage investigational product and study supplies at trial sites.
• Serve as the primary liaison between study sites and the study team.
• Provide training and support to site staff on trial protocols and procedures.
• Monitor site compliance and identify potential risks and issues.
• Implement corrective and preventive actions (CAPAs) as needed.
• Contribute to the development of study protocols and other trial-related documents.
• Ensure timely reporting of adverse events and safety information.

Qualifications:

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 5 years of experience as a Clinical Research Associate.
• Extensive experience in oncology clinical trials is mandatory.
• In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
• Proven experience with site monitoring and data management.
• Excellent communication, interpersonal, and organizational skills.
• Ability to travel to clinical sites as needed.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Strong problem-solving abilities and attention to detail.
• Ability to work independently and manage workload effectively in a remote setting.

This remote position offers a competitive salary, benefits, and the opportunity to contribute to vital cancer research.