Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead
Hybrid Clinical Trial Administrator – TMF & Site Support

Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead

Maidenhead Full-Time 30000 - 50000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Manage study documentation and support project teams in clinical trials.
  • Company: Leading clinical research organisation with a focus on innovation.
  • Benefits: Full-time role with remote work flexibility and hands-on experience.
  • Why this job: Gain valuable experience in a fast-paced environment while making a difference in oncology.
  • Qualifications: 1-2 years of experience in clinical trials, especially in oncology.
  • Other info: Opportunity for career growth in a dynamic setting.

The predicted salary is between 30000 - 50000 £ per year.

A leading clinical research organization in Maidenhead is seeking a proactive Clinical Trial Administrator. This full-time, permanent role is based in central London for at least 3 days a week, with some remote work flexibility.

Candidates should have 1-2 years of experience in clinical trials, particularly in oncology.

Responsibilities include:

  • Managing study documentation
  • Supporting project teams
  • Ensuring regulatory compliance

This role offers an opportunity to gain valuable hands-on experience in a fast-paced environment.

Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead employer: Fortrea

As a leading clinical research organization, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises employee growth and development. Our Maidenhead location offers a collaborative environment where you can thrive in your role as a Clinical Trial Administrator, with the added benefit of flexible remote work options. Join us to gain invaluable experience in the clinical trials sector, particularly in oncology, while contributing to impactful research that makes a difference in patients' lives.
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Contact Detail:

Fortrea Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead

Tip Number 1

Network like a pro! Reach out to professionals in the clinical trials field, especially those with experience in oncology. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!

Tip Number 2

Prepare for interviews by brushing up on your knowledge of TMF (Trial Master File) management and regulatory compliance. We recommend practising common interview questions and scenarios related to clinical trials to show you're ready to hit the ground running.

Tip Number 3

Don’t just apply anywhere—focus on organisations that align with your career goals. Check out our website for openings that match your skills and interests, and tailor your approach to each role to stand out from the crowd.

Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.

We think you need these skills to ace Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead

Clinical Trial Management
Oncology Knowledge
Regulatory Compliance
Documentation Management
Project Support
Proactivity
Attention to Detail
Communication Skills
Time Management
Team Collaboration
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical trials, especially in oncology. We want to see how your skills match the role, so don’t be shy about showcasing relevant projects or responsibilities you've had.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how you can contribute to our team. Keep it concise but engaging – we love a good story!

Showcase Your Attention to Detail: As a Clinical Trial Administrator, attention to detail is key. In your application, highlight any experiences where you’ve had to manage documentation or ensure compliance. We need to know you can handle the nitty-gritty!

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 – just a few clicks and you’re done!

How to prepare for a job interview at Fortrea

Know Your Stuff

Make sure you brush up on your knowledge of clinical trials, especially in oncology. Familiarise yourself with the key regulations and documentation processes involved. This will show that you're not just interested in the role but also understand the industry.

Show Your Proactivity

As a Clinical Trial Administrator, being proactive is crucial. Prepare examples from your past experience where you took initiative or solved problems. This will demonstrate your ability to support project teams effectively and manage study documentation.

Ask Smart Questions

Prepare thoughtful questions about the company’s approach to clinical trials and their specific projects. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Dress the Part

Even if the role offers some remote work flexibility, it's important to dress professionally for the interview. It sets a positive tone and shows that you take the opportunity seriously. Aim for smart-casual attire that reflects the company's culture.

Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead
Fortrea
Location: Maidenhead

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  • Hybrid Clinical Trial Administrator – TMF & Site Support in Maidenhead

    Maidenhead
    Full-Time
    30000 - 50000 £ / year (est.)
  • F

    Fortrea

    50-100
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