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- Tasks: Join our Oncology team to monitor clinical trials and support investigators.
- Company: Work with a leading global pharmaceutical company focused on innovative medicines.
- Benefits: Enjoy a collaborative environment that values your contributions and offers growth opportunities.
- Why this job: Make a real impact in healthcare while working in a supportive and empowering culture.
- Qualifications: Must have strong Oncology experience and reside in Northern England or Midlands.
- Other info: Ideal for those passionate about saving lives through clinical research.
The predicted salary is between 36000 - 60000 £ per year.
Experienced, high-performing, UK-based CRA/clinical research associate required to augment existing Oncology CRA team for pharmaceutical and biotechnology company partner. You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Your main responsibilities will include:
- Contribute to the selection of potential investigators.
- Provide the required monitoring visit reports within required timelines.
- Drive performance at the sites.
- Proactively identify study-related issues and escalate as appropriate.
- Perform source data verification according to SDV plan and ensure data query resolution.
- Initiate, monitor and close study sites in compliance with client Procedural Documents.
- Share information on patient recruitment and study site progress within local Study Delivery Team.
- Train, support and advise Investigators and site staff in study related matters.
We are looking for candidates with strong Oncology experience working in a clinical research monitoring capacity, and residing in Northern England or Midlands, UK (with appropriate right-to-work in the UK already granted, if applicable).
Clinical Research Associate - Oncology employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - Oncology
✨Tip Number 1
Network with professionals in the oncology field. Attend industry conferences, webinars, or local meetups to connect with others who work in clinical research. This can help you learn about job openings and get referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in oncology research. Being knowledgeable about current studies and breakthroughs can give you an edge during interviews and show your passion for the field.
✨Tip Number 3
Reach out to current or former employees of the company you're applying to. They can provide insights into the company culture and the specific expectations for the Clinical Research Associate role, which can help you tailor your approach.
✨Tip Number 4
Prepare for potential interview questions by practising your responses to common scenarios faced by CRAs in oncology. Think about how you would handle site monitoring challenges or patient recruitment issues, as these are likely to come up.
We think you need these skills to ace Clinical Research Associate - Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in oncology and clinical research. Focus on specific roles and responsibilities that align with the job description, such as monitoring visit reports and site performance.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and your commitment to improving patient outcomes. Mention your experience with investigator selection and data verification, and how you can contribute to the team.
Highlight Relevant Skills: In your application, emphasise skills that are crucial for the role, such as problem-solving, communication, and training abilities. Provide examples of how you've successfully navigated study-related issues in the past.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential in clinical research.
How to prepare for a job interview at ICON
✨Showcase Your Oncology Expertise
Make sure to highlight your specific experience in oncology during the interview. Discuss any relevant studies you've worked on, the challenges you faced, and how you overcame them. This will demonstrate your capability and passion for the field.
✨Understand the Company’s Portfolio
Familiarise yourself with the pharmaceutical company's portfolio, especially their oncology products. Being able to discuss their innovations and how they impact patient care will show your genuine interest and preparedness for the role.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Prepare examples of how you've proactively identified and resolved study-related issues in previous roles, as this is crucial for the position.
✨Emphasise Team Collaboration
Since the role involves working closely with investigators and site staff, be ready to discuss your experience in team settings. Highlight instances where you trained or supported colleagues, showcasing your ability to foster a collaborative environment.
