Job Title: Clinical Trial Administrator, London
Job Location: Maidenhead SL6, UK
Job Location Type: Hybrid
Job Contract Type: Contract
Job Seniority Level: Entry level
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
The role
Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is to be 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
1. Communicate with project teams and track study activities
2. Maintain essential documentation and regulatory compliance
3. Support site and study material preparation
4. Assist with meeting coordination, minute-taking, and documentation
5. Manage Trial Master File (TMF) documentation and quality control
6. Liaise with vendors and coordinate study supply shipments
7. 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!
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
Fortrea Is Proud To Be An Equal Opportunity Employer
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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