Senior Clinical Research Associate

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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
• Serve as the primary point of contact for investigators, site staff, CROs, and vendors
• Support feasibility assessments and site selection in collaboration with the study team
• Assist with the development and review of clinical documentation in including protocols, informed consent forms, monitoring plans, CRFs, and data management plans
• Support and manage patient recruitment strategies to increase enrolment and randomisation
• Review AEs and SAEs, ensuring appropriate documentation, follow‑up, and communication of safety issues
• Support data review, validation, and cleaning activities to meet study timelines
• Order and coordinate study supplies
• Develop and maintain tracking tools to support clinical trial oversight
• Plan and participate in investigator meetings and CRA trainings
• Participate in co‑monitoring activities with CRO CRAs as required
• 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
• Ability to work independently while collaborating closely with the sponsor and cross‑functional teams

Seniority level:
Associate

Employment type:

Full‑time

Job function:
Project Management