At a Glance
- Tasks: Coordinate and administer clinical studies from start-up to close-out.
- Company: Join ICON, a leader in clinical research with a commitment to innovation.
- Benefits: Enjoy a competitive salary, remote work options, and a supportive workplace culture.
- Other info: This is a permanent, full-time role based in Luton with flexible working arrangements.
- Why this job: Make a real impact in healthcare while working in a collaborative and inclusive environment.
- Qualifications: A degree in sciences or equivalent experience in clinical trials is required.
The predicted salary is between 36000 - 60000 £ per year.
*Luton - office-based position available*
Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Senior Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and a solid understanding of clinical research.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in Oncology trials.
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.
The Oncology Senior Clinical Study Administrator assists in the coordination and administration of the clinical study activities in the study start-up team, and within the Local Study Team, ensures the quality and consistency of study deliverables to time, cost and quality objectives. - Reporting into the Clinical Administration Manager, you’ll be involved in the coordination and administration of clinical studies from the start-up to execution and close-out. For this post, it is desirable that you have similar clinical trial experience within the Pharmaceutical Industry.
You will be collecting, assisting in preparation, reviewing and tracking of documents for the clinical trial application process. You’ll contribute to the production and maintenance of study documents, and be template and version compliant.
Also, you will need to translate or give the appropriate support with the translation of documents when required. Working closely with the Project Leader and CRA teams, you will be working on a number of clinical studies at any one time. You need to be comfortable working in a fast-paced environment.
#LI-DB1
Sciences degree/equivalent.
- Permanent full-time contract of employment with us and 100% embedded to one client
- Office-based in the Luton area (England): minimum 3 days per week and 2 days working from home
- Competitive salary depending on level of skills and experience plus company benefits
Snr Clinical Study Administrator - Luton employer: ICON Strategic Solutions
At ICON, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. Our Luton office provides a supportive environment where employees are empowered to grow and make meaningful contributions to life-saving clinical research. With competitive salaries, flexible working arrangements, and a strong commitment to inclusion and belonging, we ensure that every team member feels valued and has the opportunity to thrive in their career.
StudySmarter Expert Advice🤫
We think this is how you could land Snr Clinical Study Administrator - Luton
✨Tip Number 1
Familiarise yourself with the specific clinical trials and studies that ICON is currently involved in. Understanding their portfolio will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with current or former employees of ICON, especially those in similar roles. They can provide valuable insights into the company culture and expectations, which can be beneficial for your application process.
✨Tip Number 3
Prepare to discuss your experience with clinical study administration in detail. Be ready to share specific examples of how you've contributed to study start-up processes and document management in previous roles.
✨Tip Number 4
Showcase your ability to work in fast-paced environments by highlighting relevant experiences. Discuss how you’ve successfully managed multiple projects simultaneously, as this is crucial for the Senior Clinical Study Administrator role.
We think you need these skills to ace Snr Clinical Study Administrator - Luton
Some tips for your application 🫡
Understand the Role:Before applying, make sure you fully understand the responsibilities of a Senior Clinical Study Administrator. Familiarise yourself with clinical research processes and the specific requirements mentioned in the job description.
Tailor Your CV:Customise your CV to highlight relevant clinical research experience. Emphasise any previous roles that involved coordination and administration of clinical studies, as well as your understanding of the pharmaceutical industry.
Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for clinical research and your alignment with ICON's values of inclusion and belonging. Mention specific experiences that demonstrate your ability to thrive in a fast-paced environment.
Proofread Your Application:Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at ICON Strategic Solutions
✨Showcase Your Clinical Research Experience
Make sure to highlight your relevant clinical research experience during the interview. Be prepared to discuss specific projects you've worked on, your role in those projects, and how they relate to the responsibilities of a Senior Clinical Study Administrator.
✨Demonstrate Your Understanding of Clinical Trials
Familiarise yourself with the clinical trial process, including study start-up, execution, and close-out phases. Being able to articulate your understanding of these processes will show that you are well-prepared for the role.
✨Emphasise Team Collaboration Skills
Since the role involves working closely with various teams, be ready to discuss your experience in collaborative environments. Share examples of how you've successfully partnered with others to achieve common goals in previous roles.
✨Prepare Questions About Company Culture
ICON values inclusion and belonging, so prepare thoughtful questions about their culture and how they support employee development. This shows your interest in not just the role, but also in being part of their team and contributing positively to their environment.
