Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
Evaluate the quality and integrity of study site practices and manage the progress of assigned studies.

At least 1 year of independent on-site monitoring experience of interventional studies in the UK.
Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Clinical Research Associate II, Oncology

Key skills