Research Associate

Senior Clinical Research Associate (Oncology)
Working embedded with a leading global oncology-focused biopharmaceutical company
We are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role.

This position offers the opportunity to work closely with a sponsor team, supporting Phase I–III oncology studies (liquid and solid tumours) and contributing across the full clinical trial lifecycle.

Conduct routine site monitoring visits and support site selection, initiation, and close-out activities
Ensure clinical trials are conducted in accordance with GCP, ICH guidelines, approved protocols, SOPs, and regulatory requirements
Assist with the development and review of clinical documentation in including protocols, informed consent forms, monitoring plans, CRFs, and data management plans
Support data review, validation, and cleaning activities to meet study timelines
Develop and maintain tracking tools to support clinical trial oversight
Plan and participate in investigator meetings and CRA trainings
Provide guidance and support to junior CRAs as part of the wider study team

Bachelor’s degree or Registered Nurse qualification, preferably in Life Sciences
Minimum of 5 years’ experience as a Clinical Research Associate within the pharmaceutical or biotechnology industry
Experience in monitoring clinical trials from start-up through database lock
Strong oncology monitoring experience across Phase I–III trials, including liquid and solid tumours
Strong knowledge of GCP, ICH, and applicable regulatory requirements