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Clinical Programme Leader

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.


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 motivated individual with a track record of managing clinical trials across phases I, II and III , who is adept at overseeing CRO activities. Must be self-motivated, driven and proactive with strong organizational skills and able to work with limited supervision. 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.

Primary Responsibilities

  • Operational delivery of clinical development programme according to approved programme objectives, timelines, resource plan (budget, people) and quality.
  • Develop project scope, integrated cross functional plans (with highlighted critical path), timelines, budget and risk mitigation plans.
  • Overseeing the execution of clinical trial activities in accordance with Good Clinical Practices. Ensure compliance of clinical trials with national and international regulatory requirements and company SOPs.
  • Reviewing pre-study, study initiation, interim monitoring visit and at study closeout visit reports. Provides close oversight on the findings on the monitoring reports and loops back with broader team to provide updates.
  • Ensuring high performance, adherence to protocol and efficiency of the CRO clinical team and investigator sites through performing of co-monitoring /accompanied site visits. Work to proactively address trial conduct issues and enrollment problems, as necessary.
  • Maintaining the Sponsor Oversight File and the oversight of the TMF. Ensures TMF is maintained and complete at the end of the study. Perform periodic QC of the TMF
  • 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) und Standard Operating Procedures (SOPs).
  • Reviewing study metrics and manage risks for successful completion of studies. This includes reviewing study data and reports for trends and escalating issues as appropriate.
  • Support with data review activities in readiness for database lock.

We are looking for someone with

  • Ability to perform in a small dynamic company environment with an ability to work flexibly and independently.
  • Minimum of a Bachelor’s Degree in a Scientific Discipline
  • Minimum 8 years’ experience
  • Understanding of the drug development processes in the Pharma Industry environment.
  • 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 (AMS: BAI) is a leading, clinical-stage AI-enabled drug discovery and development company listed on the Euronext Amsterdam stock exchange. Through the combined capabilities of its AI platform, scientific expertise, and wet-lab facilities, BenevolentAI is well-positioned to deliver novel drug candidates with a higher probability of clinical success than those developed using traditional methods. The Benevolent Platform™ powers a growing in-house pipeline of 13 named drug programmes and over 10 exploratory programmes, and it maintains successful collaborations with AstraZeneca, as well as leading research and charitable institutions. BenevolentAI is headquartered in London, with a research facility in Cambridge (UK) and a further office in New York.

Want to do a little more research before you apply?

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