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- Tasks: Join a dynamic team to monitor clinical trials and support investigators.
- Company: Be part of a leading global biotechnology company focused on innovative healthcare solutions.
- Benefits: Enjoy a strong support structure, mentoring, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare while working in a collaborative and innovative environment.
- Qualifications: Must have over 2 years of experience as a UK clinical research monitor and 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.
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. Attend industry conferences, webinars, or local meetups to connect with current CRAs and learn about their experiences. This can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the specific requirements and responsibilities outlined in the job description. Prepare to discuss how your previous experience aligns with these tasks during the interview, especially your ability to drive performance at study sites.
✨Tip Number 3
Research the company’s recent projects and achievements in the biotechnology sector. Being knowledgeable about their work will not only impress your interviewers but also help you articulate how you can contribute to their goals.
✨Tip Number 4
Practice common interview questions for Clinical Research Associates, focusing on scenario-based questions that assess your problem-solving skills. Be ready to share specific examples from your past experiences that demonstrate your expertise in monitoring and site management.
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 therapeutic areas you've worked in, 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 training site staff. These are crucial for the role and will demonstrate your capability to meet the job requirements.
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.
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Clinical Research Basics
Make sure you brush up on your clinical research knowledge, especially the key responsibilities of a CRA. Understand the processes involved in site selection, monitoring visits, and data verification, as these will likely come up during the interview.
✨Showcase Your Experience
Be prepared to discuss your previous experience in detail. Highlight specific projects you've worked on, challenges you've faced, and how you've contributed to the success of those studies. This will demonstrate your capability and readiness for the role.
✨Understand the Company’s Mission
Research the biopharmaceutical company’s mission and values. Be ready to explain how your personal goals align with their focus on addressing unmet medical needs. This shows that you are not just looking for any job, but are genuinely interested in contributing to their cause.
✨Prepare Questions for Them
Have a list of thoughtful questions ready to ask at the end of the interview. Inquire about the team dynamics, training opportunities, or how they measure success in this role. This demonstrates your enthusiasm and interest in the position.
