Clinical Research Associate

Clinical Research Associate focuses on the clinical research associate will support oncology studies and cover sites across the uk.

What the role involves

• 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.
• Drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Work with sites to adapt.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropr.

Skills and requirements

• 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.
• Flexibility to travel to sites as required.

Candidate fit

• clinical judgement, NMC standards, calm communication, and careful documentation

Additional role context

• Chesterfield, England, United Kingdom.
• Apply today and forge a career with greater purpose, make an impact and never stop learning!