Clinical Research Associate II

About the role

A monitoring role overseeing clinical trials at investigator sites, keeping studies compliant with regulations and protecting participants and data. The position supports study teams and sponsors throughout the trial lifecycle.

What you will do

• Manage and monitor assigned clinical studies at investigative sites
• Carry out pre-study, initiation, routine monitoring and close-out visits
• Verify informed consent and protocol adherence to protect study participants
• Review source documents, raise queries and confirm data accuracy
• Check that site regulatory files and trial master documents stay complete
• Track investigational product inventory and secure storage of study materials

What they look for

• Working knowledge of ICH GCP guidelines and applicable regulations
• Experience monitoring clinical trials and managing site relationships
• Ability to review source data and resolve queries against review guidelines
• Willingness to travel, including by air, as a core part of the job
• Skill in preparing timely and accurate trip reports