1,496 Cancer Research jobs in the United Kingdom
Clinical Research Scientist
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Your responsibilities will extend to data interpretation, report generation, and contributing to scientific publications and regulatory submissions. This position requires a rigorous scientific approach, excellent analytical skills, and the ability to work independently and collaboratively within a virtual setting. You will liaise with cross-functional teams, including medical affairs, regulatory affairs, and manufacturing, to ensure seamless project progression. A strong understanding of Good Clinical Practice (GCP) and relevant regulatory frameworks (e.g., FDA, EMA) is essential. This is an exceptional opportunity to contribute to life-changing medicines and advance your career in a supportive and forward-thinking virtual environment.
Responsibilities:
- Design, develop, and manage clinical trial protocols.
- Oversee the execution of clinical studies, ensuring compliance with GCP and regulatory guidelines.
- Analyze and interpret clinical trial data to assess drug safety and efficacy.
- Prepare comprehensive study reports, scientific publications, and regulatory submissions.
- Collaborate with internal teams (e.g., R&D, regulatory, medical affairs) and external stakeholders (e.g., investigators, CROs).
- Manage budgets and timelines for assigned clinical trials.
- Identify and evaluate potential clinical investigators and sites.
- Provide scientific and technical expertise throughout the drug development process.
- Stay abreast of scientific advancements and therapeutic area developments.
- Contribute to the strategic direction of clinical development programs.
Clinical Research Scientist
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Clinical Research Scientist - Oncology
Posted today
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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.
Clinical Research Scientist - Oncology
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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.
Clinical Research Coordinator
Posted 14 days ago
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Job Title: Clinical Research Coordinator (Band 6 Nurse)
Contract Type: Part-Time (2–3 days/week)
Overview:
We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.
Key Responsibilities:
- Identify and recruit eligible patients for clinical trials.
- Perform accurate and timely data entry into study databases.
- Collaborate with research and clinical teams to ensure protocol compliance.
- Maintain high standards of documentation and regulatory adherence.
Requirements:
- Registered Band 6 Nurse with relevant clinical experience.
- Demonstrated experience in patient identification and data entry.
- Strong attention to detail and organizational skills.
- Must be available to work every Wednesday, plus two additional weekdays.
Please submit your CV or get in touch via email:
Clinical Research Physician
Posted 21 days ago
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Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Clinical Research Physician
Posted 21 days ago
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Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
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Clinical Research Coordinator
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URGENT HIRING: Clinical Research Coordinator – Bath
I'm reaching out with an exciting full-time opportunity for a Clinical Research Coordinator (CRC) to join a global clinical research service provider supporting multiple sponsors.
Therapeutic Area: Atopic Dermatitis (experience required)
Location: On-site in Bath
Start Date: ASAP
Duration: Until October (potential to extend)
This role is ideal for a Band 5/6 Nurse or Clinical Research Nurse ready to step into a CRC title.
Key Responsibilities:
- Patient identification & chart reviews
- Referral physician networking
- Community outreach
Preferred Experience:
- Background in nursing or clinical research
- Familiarity with Millennium Sauna or other EDC systems
Clinical Research Associate
Posted today
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Are you a passionate CRA II or Senior CRA looking for your next challenge?
We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusively with a leading Pharmaceutical client.
This is a unique opportunity to be part of a dynamic and supportive environment where your contributions directly impact the future of medicine. Our clients FSP model provides the stability and support of a dedicated team, while you gain exposure to the innovative research of a top-tier pharmaceutical company.
About the role:
As a CRA II or Senior CRA, you will be responsible for the full range of monitoring activities, from site initiation to close-out. You'll ensure the highest standards of data quality and compliance with ICH-GCP, protocols, and all applicable regulations. This role is home-based and will involve travel to sites across your designated region.
What our client offer:
- Salary: £45,000 - £55,000 per annum, depending on experience.
- Car/Car Allowance: A company car or a competitive car allowance.
- Bonus & Benefits: An attractive bonus scheme and a comprehensive benefits package.
- Career Growth: We are committed to your professional development and offer extensive training, mentorship, and opportunities for progression within our growing FSP.
Location:
This is a home-based role to be based in one of the following regions:
- North England
- North West England
- Midlands
- London
- South England
Requirements:
- Proven experience as a CRA, with a strong understanding of the clinical trial lifecycle. 18 months minimum as a CRA to be CRAII and 3 year + to be considered for Senior CRA.
- Excellent knowledge of ICH-GCP guidelines and relevant regulations.
- Strong communication and interpersonal skills.
- A proactive and independent approach to your work.
- A full UK driving licence and willingness to travel.
If you are ready to take the next step in your career and join a company that values growth, training, and support, we want to hear from you.
Apply now or message us for more details!
#CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global
Clinical Research Associate
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Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)
Location: Hybrid UK Based
Employment Type: Freelance
Function: Clinical Operations
Therapeutic Area: Oncology
Reports To: Clinical Operations Manager
About the Role
We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.
Key Responsibilities
- Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
- Assist in site selection and feasibility assessments.
- Ensure proper documentation and timely resolution of site issues.
- Support site staff in understanding and complying with study protocols and GCP guidelines.
- Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
- Ensure timely collection and review of essential regulatory documents.
- Track patient recruitment and retention efforts at assigned sites.
- Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
- Maintain high-quality communication with clinical sites and sponsor/CRO teams.
- Escalate site performance or compliance issues as needed.
Required Qualifications
- Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
- Exposure to oncology trials (academic, site, or CRO experience).
- Understanding of ICH-GCP guidelines and regulatory requirements.
- Strong organizational skills with attention to detail.
- Ability to manage multiple tasks and priorities independently.
- Excellent communication and interpersonal skills.
- Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.