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Jobs at Parexel

We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it With Heart ™.

Clinical Trials Associate (FSP)

Job ID 83545BR United Kingdom - Any Region - Home Based

Play a pivotal role in some of the most significant clinical studies taking place today. Work with world-renowned sponsors, including the top 50 pharmaceutical companies. Collaborate, and learn, alongside some of the industry’s most experienced people.

Working as a Clinical Trials Administrator at Parexel FSP provides an exciting platform for your skills, as well potential to develop into roles such as trial manager, project leader, In-house CRA or clinical research associate.

We make a difference to millions of lives. We’ll do the same for your career!

Specific to this advertised role…
  • Opportunity to enter the clinical research field.
  • You could be assigned to support early phase or late phase projects.
  • Opportunity to work with sites, study teams, Field Clinical Research Associates (CRAs) and vendors.
  • Gain insight into varied therapeutic areas.
  • Home-based.
  • Work with a global or international team (dependant on client).

Clinical Trials Administrator

Our Clinical Trials Administrators are valued members of our clinical studies teams. They assist the project team in running clinical trials successfully from beginning to end.

Their contribution includes maintaining trial master files and systems, checking, collecting and managing vital documentation, undertaking supply activities and liaising with colleagues and partners site-wide.

But it’s not just about the nuts and bolts of administration. Your expertise and advice will be welcome in key deliberations, such as preparations for study set up, and the conduct and close out of Clinical studies

Most of our Clinical Trials Administrator roles are home-based. Typically, you’d be supporting between 1 and 4 trials (depending on their size and complexity).

You’ll be part of a highly supportive CTA organisation. Your fellow Administrators and Managers are only ever a phone call away for help, information, or advice.

At Parexel FSP we believe strongly in work/life balance we’ll take your well-being just as seriously as we do that of our patients.

To us, that’s what ‘working with heart’ is all about.


What you’ll need to join us as a Clinical Trials Administrator

Clinical Trials Administration experience gained within CRO or Pharma is ideal, but you could equally be working in a related field, such as academia.

We’ll provide a comprehensive induction programme to get you up to speed with our systems and approach. And then we’ll mentor and support you at every stage.

Here are the typical skills and knowledge we look for, together with any requirements specific to this advertised job: -
  • A minimum of 1 year’s clinical trial experience, preferably within the pharmaceutical or biotechnology industry.
  • Basic knowledge and understanding of Essential Documents, CFR, and GCP/ICH.
  • Proficiency with technological systems (Microsoft Office, TMF, CTMS, EDC, ECMS, Zoom/Teams).
  • Fundamental understanding of filing systems and organizational tools.
  • Ability to manage multiple and varied tasks, and to prioritize workload, with attention to detail.

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