Clinical Research Associate

As a Clinical Research Associate, the work centres on the Clinical Research Associate will support Oncology studies and cover sites across the UK. It would suit someone who can bring patience, clear communication, and care for residents or service users to the role.

Known job details

• Contract: Full-time
• Work model: On-site
• Additional detail: Training or development support may be provided.

Likely focus of the role

• The Clinical Research Associate will support Oncology studies and cover sites across the UK.
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Driving, and track subject recruitment plan in line with project needs to enhance predictability.

Requirements mentioned

• Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Life science degree educated or equivalent industry experience.