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Clinical
London

Clinical Trial Assistant

With over 35 nationalities and a range of backgrounds represented in our Benevolent team, we aim to build an inclusive environment where our people can bring their authentic selves to work, be respected for who they are and the exceptional work they do. We welcome and actively encourage applications from all sections of society and are committed to offering equal employment opportunities regardless of sex, race, religion or belief, ethnic or national origin, marital, domestic or civil partnership status, sexual orientation, gender identity, parental status, disability, age, citizenship, or any other basis. We see our diversity as an asset as we tackle challenging problems that bridge the gap between drug discovery and technology.

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The Role

This is an exciting opportunity to join an expanding group supporting a growing pipeline of clinical projects. The team is looking for a freelance clinical trial assistant (CTA) with a track record of supporting clinical trials across phases I, II and III. Must be self-motivated, driven and proactive with strong organizational skills and able to work with limited supervision.

Experience with the DIA TMF reference model is required.

Reporting to the Director Clinical Programme Leader, the successful candidate will manage the activities of suppliers to deliver high-quality studies on time and to budget.

This is an initial 3 month fixed-term contract.

Primary Responsibilities

  • Maintenance of paper and electronic Trial Master Files: Maintain sponsor sections of TMF, Periodic QC of sponsor sections of TMF and eTMF using the DIA reference model, Synchronising paper TMF and electronic project files, Ensure consistency of project files across clinical projects, Support QC of supplier TMF and eTMF using the DIA reference model.
  • Maintenance of all sponsor tracking of clinical studies
  • Management of the TMF archiving process and ensuring that TMF is archived at the end of the trial in compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs).

We are looking for someone with

  • Ability to perform in a small dynamic company environment with an ability to work flexibly and independently.
  • 2+ years’ industry experience
  • Minimum three A’ levels or equivalent, preferably to include a science subject. Education in a science discipline to degree level preferred.
  • Excellent communication skills, able to collaborate with internal and external colleagues at all levels

We share a passion for being part of a mission that matters, and we are always looking for curious and collaborative people who share our values and want to be part of our journey.  If that sounds like a fit for you, hit the apply button and join us.

About us

BenevolentAI unites AI with human expertise to discover new and more effective medicines. Our unique computational R&D platform spans every step of the drug discovery process, powering an in-house pipeline of over 25 drug programmes. We advance our mission to reinvent drug discovery by harnessing the power of a diverse team, rich with different backgrounds, experiences, opinions and personalities.  In our offices in London and New York and research facility in Cambridge (UK), we work in highly collaborative, multidisciplinary teams, harnessing skills across biology, chemistry, engineering, AI, machine learning, informatics, precision medicine and drug discovery.

Want to do a little more research before you apply?

Head over to our Glassdoor page to learn about our benefits, culture and to find out what our team think about life at Benevolent. You can also find out more about us on LinkedIn and Twitter.

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Important Note

Our team will only contact you from the domain @benevolent.ai. If you receive a suspicious contact request, please email hello@benevolent.ai. Thank you.