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For Companies At a Glance
- Tasks: Assist in coordinating and administering clinical trials while ensuring compliance with protocols.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and a supportive work-life balance.
- Why this job: Make a real impact in clinical research and help shape the future of healthcare.
- Qualifications: Bachelor's degree in a scientific field and a keen interest in clinical research.
- Other info: Inclusive culture with opportunities for personal and professional growth.
The predicted salary is between 30000 - 50000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are currently seeking a Clinical Trial Associate to start immediately in the Cambridge area (UK). You will join our dynamic team and play a pivotal role in assisting with the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
What You Will Be Doing
- Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials, such as informed consent forms and case report forms.
- Responsible for study start-up activities, including creating site folders, collating, preparing and maintaining (e) SIP documents, and updating systems.
- Liaise with clinical sites to collect, review and track feasibility questionnaires.
- Co-ordinate entry and maintain local data into study management systems (eClinical, CDSS/CDSSR, SADMS, etc.) including setting up new studies in eClinical.
- Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contribute to the tracking and reporting of clinical trial metrics and milestones.
Your profile
- Bachelor's degree in a scientific or healthcare-related field.
- Prior experience or strong interest in clinical research.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with attention to detail.
What ICON Can Offer You
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits focused on well-being and work-life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Clinical Trial Associate in Reading employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Associate in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching ICON plc and understanding their mission and values. Tailor your responses to show how your skills align with their goals. We want to see your passion for clinical trials and how you can contribute to their success!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your answers. Focus on articulating your experience in clinical research and how it relates to the role of a Clinical Trial Associate.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us. So, get that application in and let’s shape the future of clinical development together!
We think you need these skills to ace Clinical Trial Associate in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trial Associate role. Highlight any relevant experience or skills that match the job description, like your knowledge of clinical trial processes and regulations. We want to see how you fit into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for us. Keep it concise but engaging – we love a good story!
Showcase Your Organisational Skills: Since this role involves a lot of coordination and documentation, make sure to highlight your organisational skills in your application. Share examples of how you've successfully managed multiple tasks or projects in the past – we appreciate attention to detail!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the info you need about the role and our company culture there!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trial processes, regulations, and guidelines. Familiarise yourself with the specific protocols that ICON plc follows, as this will show your genuine interest in the role and help you answer questions confidently.
✨Organise Your Documentation Skills
Since you'll be maintaining and organising clinical trial documentation, it’s a good idea to prepare examples of how you've successfully managed similar tasks in the past. Bring along any relevant documents or reports that showcase your organisational skills.
✨Showcase Your Teamwork
Collaboration is key in this role, so think of instances where you've worked effectively within a team. Be ready to discuss how you facilitated communication and contributed to smooth project execution, especially in fast-paced environments.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the team dynamics, ongoing projects, or the company culture at ICON. This not only shows your enthusiasm but also helps you gauge if it's the right fit for you.