Clinical Data Analyst

Clinical Data Analyst

London Full-Time 31445 - 36410 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage and analyse clinical trial data, supporting the Senior Clinical Data Analyst.
  • Company: Join the Institute of Cancer Research, a leading global cancer research institute.
  • Benefits: Enjoy exclusive staff benefits and flexible office work options.
  • Why this job: Be part of groundbreaking Phase-I cancer trials and make a real impact in healthcare.
  • Qualifications: Degree in life science or nursing; knowledge of clinical trials is a plus.
  • Other info: One-year fixed-term contract; apply early as positions may close before the deadline.

The predicted salary is between 31445 - 36410 Β£ per year.

Salary: Β£31,445 - Β£36,410. Commencement on the salary range is subject to comparable skills and experience.

Duration of Contract: Fixed Term for 12 months

Hours per week: 35 hours per week (Full Time)

Closing Date: 9th July 2025

The Institute of Cancer Research is looking for a Clinical Data Analyst to work in the Investigator Initiated Trials (IIT) Team, which is part of the Drug Development Unit (DDU). The post offers an enthusiastic and well-motivated individual a chance to work in a motivated and supportive academic team that are at the forefront of Phase-I cancer trials.

The Drug Development Unit, within the ICR and Royal Marsden, is a dedicated Clinical Trials Unit, with bespoke facilities to conduct early phase clinical trials. The Unit, led by Professor Johann de Bono, comprises Drug Development Unit – Investigator Initiated Trials team which aims to seamlessly integrate preclinical drug discovery, proof-of-principle phase I trials and tumour-specific evaluation of novel agents. It is a conduit for the two-way communication between laboratory and clinical teams that is so essential for successful modern drug development.

The unit conducts first-in-man phase I trials involving a range of targets, including growth factor or intracellular signalling, angiogenesis, apoptosis, epigenetics and DNA repair. All trials are underpinned by extensive analysis of biomarkers, both predictive and pharmacodynamics. The DDU includes The Oak Foundation Drug Development Centre (Oak Ward) housed within The Royal Marsden at the Sutton site and specifically designed for phase I clinical trials. Opened in February 2005, the centre provides 10 inpatient beds, five treatment chairs and two outpatient suites, and allows researchers to enter almost 300 patients onto phase I trials each year. This makes the unit one of the largest of its kind in the world.

The DDU also has a portfolio of investigator-initiated phase 1 trials (IIT’s) of novel targeted agents and combinations of these, including those made available via Cancer Research-UK’s (CRUK) Experimental Cancer Medicine Centres (ECMC) Combinations Alliance. These studies are centrally managed by the IIT team within the DDU that performs those functions associated with sponsoring early phase trials including project management, monitoring, pharmacovigilance, database development and central data review. The successful applicant will support the Senior Clinical Data Analyst in overseeing data management activities of the IIT team.

Summary Of Role

The post holder will be responsible for managing the data collected during a clinical trial. This will include designing the database used to collect the data, reviewing the data that is collected, and analysing the data by creating data tables for reports and publications. The role will also involve supporting the Senior Clinical Data Analyst in overseeing data management activities of the IIT team. This role is office based with some flexibility.

Key Requirements

We are looking for an individual with a passion for data and enthusiasm to fit into a forward thinking Phase I team, working on novel approaches to cancer treatments. The successful candidate must be educated to a degree level in life science or nursing. They should have excellent interpersonal skills and the ability to prioritise and manage workload as an essential skill. It is also desirable that the applicant has knowledge of clinical trials or oncology, and has an understanding of ICH-GCP (Directive 2001/20/EC and 2005/28/EC).

We encourage all applicants to access the job pack attached for more detailed information regarding this role.

Additional Information

Appointments will be on a one-year contract in the first instance. To apply for this post, please submit an online application including a supporting statement, detailing reasons why you are applying for the post and attach your CV. Due to the high volumes of applications we receive, we reserve the right to close the advert before the published closing date once we have received a sufficient number of applications. Therefore, we advise that you to submit your application, as early as possible to avoid disappointment. For an informal discussion regarding the role, please contact Toby Prout via email.

About The Institute Of Cancer Research

As a member of staff, you will have exclusive access to a range of staff benefits. The ICR is committed to supporting overseas applicants applying for roles. The Institute of Cancer Research, London, is one of the world's most influential cancer research institutes, with an outstanding record of achievement dating back more than 100 years. Further information about working at the ICR can be found here. We look forward to receiving applications from all candidates, wherever in the world they are currently based. We will select those who display the potential to become, or to support, the world leading cancer researchers of the future based on their application and performance at interview. However, we particularly welcome British applicants from black and ethnic minority backgrounds, as they are under-represented within the ICR and nationwide in STEM roles.

Clinical Data Analyst employer: The Institute Of Cancer Research

The Institute of Cancer Research is an exceptional employer, offering a dynamic and supportive work environment for Clinical Data Analysts within the pioneering Drug Development Unit. Employees benefit from a culture of collaboration and innovation, with access to cutting-edge facilities and opportunities for professional growth in the field of cancer research. Located at the Royal Marsden in Sutton, the institute not only champions diversity but also provides a unique chance to contribute to groundbreaking phase I clinical trials that have a real impact on patient care.
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Contact Detail:

The Institute Of Cancer Research Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Clinical Data Analyst

✨Tip Number 1

Familiarise yourself with the latest trends in clinical data analysis and oncology. This will not only help you understand the role better but also allow you to engage in meaningful conversations during interviews, showcasing your passion for the field.

✨Tip Number 2

Network with professionals in the clinical trials sector, especially those involved in Phase I trials. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the work being done at the Institute of Cancer Research.

✨Tip Number 3

Prepare to discuss your experience with data management and analysis tools. Be ready to provide examples of how you've successfully managed data in previous roles, as this will demonstrate your capability to support the Senior Clinical Data Analyst effectively.

✨Tip Number 4

Reach out to current or former employees of the Institute of Cancer Research via LinkedIn. Ask them about their experiences and any tips they might have for standing out in the application process, which can give you valuable insights into the company culture.

We think you need these skills to ace Clinical Data Analyst

Data Management
Database Design
Data Analysis
Statistical Software Proficiency
Knowledge of Clinical Trials
Understanding of ICH-GCP Guidelines
Interpersonal Skills
Project Management
Attention to Detail
Report Writing
Time Management
Problem-Solving Skills
Communication Skills
Team Collaboration

Some tips for your application 🫑

Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Clinical Data Analyst position. Tailor your application to highlight how your skills and experiences align with the specific needs of the Institute of Cancer Research.

Craft a Compelling Supporting Statement: In your supporting statement, clearly articulate your reasons for applying. Discuss your passion for data and any relevant experience in clinical trials or oncology. Make sure to connect your background to the role's key requirements, such as your degree in life science or nursing.

Highlight Relevant Skills: Emphasise your interpersonal skills and ability to manage workloads effectively. If you have knowledge of ICH-GCP guidelines or experience with database management, be sure to include these details in your CV and supporting statement.

Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role that involves data management.

How to prepare for a job interview at The Institute Of Cancer Research

✨Know Your Data

As a Clinical Data Analyst, it's crucial to demonstrate your understanding of data management in clinical trials. Be prepared to discuss your experience with database design and data analysis, as well as any specific tools or software you have used.

✨Show Enthusiasm for Oncology

The role is centred around cancer research, so express your passion for oncology and how it drives your work. Familiarise yourself with current trends in cancer treatments and be ready to discuss how your background aligns with the goals of the Investigator Initiated Trials team.

✨Highlight Interpersonal Skills

Excellent interpersonal skills are essential for this position. Prepare examples of how you've effectively communicated and collaborated with team members in previous roles, especially in high-pressure environments like clinical trials.

✨Understand ICH-GCP Guidelines

Knowledge of ICH-GCP guidelines is desirable for this role. Brush up on these regulations and be ready to explain how they impact data management and trial conduct, showcasing your commitment to compliance and quality in clinical research.

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