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- Tasks: Join our Oncology CRA 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 with opportunities for remote work and personal growth.
- Why this job: Make a real impact in saving lives while thriving in a culture of belonging and empowerment.
- Qualifications: Must have strong Oncology experience in clinical research monitoring and reside in Northern England or Midlands.
- Other info: This role offers flexibility and the chance to work with a well-known partner in healthcare.
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 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.
Amongst other tasks, your main responsibilities will be to;
- 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)
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Clinical Research Associate - Oncology 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
✨Tip Number 1
Make sure to highlight your specific experience in oncology during any networking opportunities. Connect with professionals in the field through LinkedIn or industry events, and discuss your background and interest in clinical research.
✨Tip Number 2
Familiarize yourself with the latest trends and innovations in oncology clinical trials. Being knowledgeable about current studies and advancements can help you stand out during conversations with potential employers.
✨Tip Number 3
Consider reaching out to current or former employees of the company you're applying to. They can provide valuable insights into the company culture and expectations, which can help you tailor your approach.
✨Tip Number 4
Prepare for potential interviews by practicing responses to common CRA scenarios, especially those related to site monitoring and investigator training. This will help you demonstrate your expertise and problem-solving skills effectively.
We think you need these skills to ace Clinical Research Associate - Oncology
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience in oncology and clinical research monitoring. Use specific examples from your past roles that demonstrate your ability to contribute effectively to the CRA team.
Tailor Your CV: Customize your CV to align with the job description. Focus on your skills in site management, monitoring visit reports, and data verification, as these are key responsibilities for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and your commitment to improving patient outcomes. Mention how your values align with the company's mission of saving lives.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no grammatical errors or typos, as attention to detail is crucial in clinical research.
How to prepare for a job interview at ICON Strategic Solutions
✨Showcase Your Oncology Experience
Make sure to highlight your specific experience in oncology during the interview. Discuss any relevant studies you've worked on and how they relate to the responsibilities of the role.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your approach to monitoring clinical trials. Share examples of how you've driven performance at study sites and resolved issues proactively.
✨Emphasize Team Collaboration
Since this role involves working closely with investigators and site staff, illustrate your ability to collaborate effectively. Talk about past experiences where you trained or supported team members.
✨Understand the Company’s Portfolio
Research the pharmaceutical company’s portfolio, especially in oncology. Being knowledgeable about their products and pipeline can help you align your answers with their goals and demonstrate your genuine interest.
