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- Tasks: Join a dynamic team to monitor clinical trials and support investigators in groundbreaking research.
- Company: Be part of a leading global biotechnology company focused on addressing unmet medical needs.
- Benefits: Enjoy a strong support structure, mentoring, and the chance to make a real impact.
- Why this job: This role offers a unique opportunity to contribute to innovative healthcare solutions while growing your career.
- Qualifications: Must have over 2 years of CRA experience and reside in the UK with a valid driving license.
- Other info: Only one internal interview required with immediate feedback!
The predicted salary is between 36000 - 60000 £ per year.
Experienced UK-based Regional CRA/clinical research associate required to augment existing CRA team for a multinational biopharmaceutical company partner. You will be part of an innovative and global Biotechnology company, who pride themselves on being one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.
This is a rewarding and interesting position with a key Global client, with a strong internal support structure in place (including a mentoring training plan) in a big team of ICON staff. For this role, there is a requirement for 1x internal interview only (and immediate feedback).
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.
Requirements:
- Strong experience (~>2 years') working as a UK clinical research monitor (or CRA).
- Resident within the UK (with appropriate right-to-work in the UK already granted, if applicable).
- Driving License.
Clinical Research Associate (I, II, Senior) - UK 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 (I, II, Senior) - UK
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work as CRAs. Attend industry events or join online forums to connect with others and learn about potential job openings.
✨Tip Number 2
Familiarise yourself with the specific requirements and responsibilities outlined in the job description. This will help you tailor your conversations during networking or interviews to demonstrate your understanding of the role.
✨Tip Number 3
Prepare for the internal interview by researching the company’s recent projects and achievements in the biotechnology sector. Showing that you are informed about their work can set you apart from other candidates.
✨Tip Number 4
Consider reaching out to current or former employees of the company on platforms like LinkedIn. They can provide insights into the company culture and the CRA role, which can be invaluable during your interview.
We think you need these skills to ace Clinical Research Associate (I, II, Senior) - UK
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Focus on your monitoring experience, any specific studies you've worked on, and your ability to drive performance at study sites.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the biopharmaceutical industry. Mention your experience with investigator selection and site management, and how you can contribute to the team.
Highlight Relevant Skills: In your application, emphasise skills such as source data verification, problem-solving, and communication. These are crucial for the role and will demonstrate your capability to handle the responsibilities outlined in the job description.
Prepare for the Interview: Since there is only one internal interview, prepare thoroughly. Review common CRA interview questions, be ready to discuss your previous experiences, and think about how you can address potential study-related issues proactively.
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical research processes and regulations. Be prepared to discuss your experience with monitoring visits, source data verification, and how you've handled study-related issues in the past.
✨Showcase Your Problem-Solving Skills
During the interview, highlight specific examples where you've proactively identified and resolved issues at study sites. This will demonstrate your ability to drive performance and ensure compliance with client procedural documents.
✨Familiarise Yourself with the Company
Research the biopharmaceutical company and its focus areas. Understanding their mission to address unmet medical needs will help you align your answers with their values and show genuine interest in the role.
✨Prepare Questions for Your Interviewers
Think of insightful questions to ask about the team dynamics, training opportunities, and the mentoring plan mentioned in the job description. This shows that you're engaged and eager to learn more about the position and the company culture.
