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- Tasks: Manage clinical trials, ensuring data integrity and patient safety while travelling to study sites.
- Company: Join ICON, a leading clinical research organisation shaping the future of healthcare.
- Benefits: Enjoy competitive salary, health insurance, retirement planning, and flexible work-life balance.
- Why this job: Make a real impact in oncology research while gaining valuable experience in a dynamic environment.
- Qualifications: Must have oncology experience and knowledge of clinical trial processes.
- Other info: Diversity and inclusion are at our core; we welcome all qualified applicants.
The predicted salary is between 36000 - 60000 £ per year.
ICON Strategic Solutions is a world‑leading clinical research organization that is looking for a Clinical Research Associate (CRA) with oncology experience. Join our journey to shape the future of clinical development.
Role
Reporting to the Clinical Research Associate Group Head, the CRA will manage the day‑to‑day activities across the study portfolio. The position requires the CRA to be based in the UK and to travel nationally (and occasionally internationally) to study sites.
Location: United Kingdom – nationwide travel required.
Travel: Minimum 50% overnight travel; domestic trips to study sites, training and meetings.
Your Responsibilities
- Site selection: evaluate potential sites for capacity to conduct clinical trials and recommend them for inclusion.
- Conduct Site Initiation Visits (SIVs), ensuring all personnel are trained and that amendments are implemented.
- Perform continuous on‑site and remote monitoring activities in compliance with GCP, ICH, FDA, EMEA and client procedures.
- Ensure data integrity and patient safety, update all electronic systems as required, and maintain accurate study documentation.
- Manage study milestones (startup, recruitment, database analysis, close‑out) and ensure on‑time delivery.
- Document monitoring activities, assist in contingency plans, and support audit and inspection readiness.
- Resolve site issues, support data query resolution, and maintain the Investigator Folder and Site Trial Master File.
- Negotiate investigator remuneration and prepare financial contracts.
You Must Have
- Right to work in the UK.
- Up to 2 years of experience in the pharmaceutical/CRO industry.
- Good knowledge of the drug development process, especially clinical trial research.
- Familiarity with international standards (GCP/ICH, FDA, EMEA).
- Minimum 12 months of monitoring experience.
Important For the Role
- Ability to travel domestically (and occasionally internationally) as required.
- Expectations of 50% overnight travel.
What ICON Can Offer You
ICON prioritises its people, offering a competitive salary and a comprehensive benefits package designed to support well‑being and work‑life balance.
Benefits Examples
- Annual leave entitlements.
- Health insurance options for you and your family.
- Retirement planning and contributions.
- Global Employee Assistance Programme.
- Life assurance.
- Optional benefits such as childcare vouchers, bike purchase schemes, gym memberships, subsidised travel passes, and health assessments.
At ICON, diversity, inclusion and belonging are fundamental to our culture and values. We are committed to building an inclusive environment free from discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you need a reasonable accommodation for any part of the application process, please let us know through the form below.
Clinical Research Associate - Oncology experience required in Reading employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - Oncology experience required in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those with oncology experience. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP, ICH, and the drug development process. We want you to shine when discussing your monitoring experience and how it relates to the role!
✨Tip Number 3
Showcase your flexibility and willingness to travel. Since this role involves a lot of site visits, let potential employers know you're ready to hit the road and manage your time effectively.
✨Tip Number 4
Apply through our website for the best chance at landing the job! We love seeing candidates who take the initiative to connect directly with us. Plus, it shows you're serious about joining our team.
We think you need these skills to ace Clinical Research Associate - Oncology experience required in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your oncology experience and relevant skills. We want to see how your background aligns with the role, so don’t be shy about showcasing your achievements in clinical trials!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your experience makes you the perfect fit for us. Keep it engaging and personal – we love a good story!
Showcase Your Monitoring Experience: Since monitoring is key for this role, make sure to detail your monitoring experience clearly. We want to know how you've ensured data integrity and patient safety in past projects, so give us the specifics!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and you’ll be set!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Familiarise yourself with the latest trends and developments in cancer research, as well as any specific trials that might be relevant to the role. This will show your passion for the field and your commitment to staying informed.
✨Demonstrate Your Monitoring Experience
Since the role requires at least 12 months of monitoring experience, be ready to discuss your past experiences in detail. Prepare examples of how you've managed site visits, resolved issues, and ensured compliance with GCP and ICH standards. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Show Off Your Travel Flexibility
With a minimum of 50% overnight travel expected, it's crucial to convey your willingness and ability to travel. Share any previous experiences where you’ve had to travel for work, and highlight how you manage your time and responsibilities while on the road.
✨Prepare Questions for Them
Interviews are a two-way street, so come prepared with thoughtful questions about the company culture, team dynamics, and the specific projects you might be working on. This not only shows your interest but also helps you determine if the company is the right fit for you.
