At a Glance
- Tasks: Support clinical trials by managing documentation and coordinating with project teams.
- Company: Fortrea, a leading company in clinical research based in central London.
- Benefits: Gain hands-on experience, work in a dynamic team, and enjoy flexible working arrangements.
- Other info: Office-based 3 days a week with excellent career growth opportunities.
- Why this job: Make a real impact in healthcare while developing your skills in a fast-paced environment.
- Qualifications: 1-2 years of clinical research admin experience and a basic understanding of biology.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is office based in central London for at least 3 days a week with the rest of the time being spent working from home. Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK. Much of the work will involve complex oncological clinical trials, providing valuable opportunities to develop your skills and expertise.
What You\\\'ll Do
- Communicate with project teams and track study activities
- Maintain essential documentation and regulatory compliance
- Support site and study material preparation
- Assist with meeting coordination, minute-taking, and documentation
- Manage Trial Master File (TMF) documentation and quality control
- Liaise with vendors and coordinate study supply shipments
- Provide general administrative and systems support
Requirements
- A minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - this is essential!
- Must be within commuting distance of Central London (office-based 3 days per week)
- Basic understanding of biology and biological processes
- Good organizational and time management skills
This role is a full time & permanent position to be employed through Fortrea.
This is a great opportunity to gain hands-on experience in clinical research and contribute to high-quality clinical data production. If you thrive in a fast-paced environment and enjoy working with a dynamic team, we\\\'d love to hear from you!
Learn more about our EEO & Accommodations request here.
Clinical Trial Administrator, London in Thatcham employer: Fortrea
Fortrea is an exceptional employer that fosters a collaborative and dynamic work environment in the heart of London. With a strong focus on employee development, we offer valuable opportunities for growth within the clinical research field, particularly in complex oncological trials. Our flexible working arrangements, combining office presence with remote work, ensure a healthy work-life balance while contributing to meaningful advancements in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Administrator, London in Thatcham
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about opportunities at Fortrea. A friendly chat can sometimes lead to a foot in the door.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of clinical trials and oncology. We want you to feel confident discussing your experience and how it relates to the role of Clinical Trial Administrator.
✨Tip Number 3
Showcase your organisational skills during the interview. Bring examples of how you've managed documentation or coordinated meetings in past roles. This will demonstrate that you're ready to handle the responsibilities of the job.
✨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 connect with us directly.
We think you need these skills to ace Clinical Trial Administrator, London in Thatcham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in clinical trials. We want to see how your skills match the role, so don’t be shy about showcasing your achievements!
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 you can contribute to our team. Keep it concise but impactful!
Showcase Your Organisational Skills:Since this role involves managing documentation and coordinating meetings, make sure to mention any relevant experiences that demonstrate your organisational prowess. We love a well-structured application!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Fortrea
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials, especially in oncology. Familiarise yourself with the latest trends and regulations in the field. This will not only show your passion but also your commitment to the role.
✨Showcase Your Organisational Skills
As a Clinical Trial Administrator, you'll need to juggle multiple tasks. Prepare examples from your past experience where you've successfully managed documentation or coordinated meetings. Highlighting your organisational prowess will impress the interviewers.
✨Prepare for Scenario Questions
Expect questions that assess how you would handle specific situations, like managing TMF documentation or liaising with vendors. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about the team dynamics or the types of trials you'll be working on. This shows your genuine interest in the role and helps you gauge if it's the right fit for you.
