We are currently looking for a self-driven Trial Data Manager to take full ownership of global clinical trials within the oncology space.

Role

This role is designed for a lead professional who can work independently without regular guidance, adding significant value to discussions with customers and clinical stakeholders. You will be responsible for the entire trial level milestone map, creating detailed project plans and negotiating timelines effectively across all functional areas.

Experience

A primary requirement for this position is hands-on technical execution. You must have direct experience with Veeva study builds, including the configuration of edit checks and form dynamics. We are looking for a candidate who ensures the database architecture is robust from the initial start-up phase through to the final lock.

This is not a specification-only role; you must be able to lead the technical configuration and provide the customer with confidence that the trial is being managed with foresight and precision.

Your expertise will also cover strong data review for safety data within oncology studies. This includes an in-depth understanding of SDTM mapping and the oversight of adverse events, serious adverse events, concomitant medications, and medical history. You will be expected to identify potential risks before they impact milestones and drive complex data tasks to successful closure under tight global timelines.

With 10 years plus experience within CRO and/or Pharmaceutical Manufacturing environments as a Lead Clinical Data Manager, you will have a proven track record of proactive communication and ownership. You should be comfortable acting as the primary point of contact for the customer and clinical teams, demonstrating the ability to work independently while ensuring all project goals are met.

This is a fully remote contract opportunity available for candidates based in either the UK or the USA.