Clinical Trial Administrator, London

2 months ago

Maidenhead, United Kingdom Fortrea Full time

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. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
- Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in London. For this particular role we are ideally looking for a ‘career’ clinical research administrator who does not wish to progress to a CRA or Project Management role.This client-dedicated role is to be office based in central London for at least 2 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 and so there is plenty of interesting (and worth while) work to get your teeth stuck intoEssential Job Duties:
- Act as contact for project team and study sites
- Perform CRF review against established data review guidelines, under direct supervision on management systems
- Assist with the management of study supplies and organize shipments
- Create, update, track, and maintain study-specific trial management files, tools, and systems.
- Assist the local project team members with other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings)
- Coordinate meetings with clients, investigators, and project team, including taking minutes.
- Ensure compliance with Fortrea SOPs, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work
- Provide input in writing Monitoring Conventions as assigned
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities
- Requirements:
- a minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - This is essential
- You must live in commuting distance of Central London, again essential.
- Basic understanding of biology and biological processes
- Good organizational and time management skills
- Other Information: This role is a full time & permanent position to be employed through Fortrea. For more information please contact Magdalena Kozłowska at-
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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