Clinical Research Associate

Clinical Research Associate II & Clinical Research Associate III

An opportunity to join a leading CRO.

This company have a strong tailored training and development programme specifically to help progression across clinical operations. They have a strong portfolio, especially across oncology, and so offer a magnitude of unique and complex studies - partnering with world leading sponsors.

They are hiring for a CRA II, and CRA III- depending on experience level.

This role is suitable for someone with at least 6 months independent monitoring experience, in a CRO or Pharmaceutical company.

Key Responsibilities :

• Working on global clinical trials across phases I-III, across oncology, cardiovascular, neurology and other therapeutic areas.
• Independently conduct regular site visits, this includes site selection, initiation, monitoring, through to close out and database lock.
• Responsible for ensuring correct clinical documentation, such as CRF, to ensure sites are compliant in line with relevant industry guidelines.

Required Skillset :

Confirmed Title and Salary :

This company will be conducting interviews in the coming weeks and so do not hesitate to apply if you are interested. Please send your CV to Keeley Munday at , or apply directly here.

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