London-Based CRA I/II: Site Monitoring & Compliance

A global clinical research company in London is looking for a Single Sponsor CRA I / II. This role involves monitoring clinical trial sites to ensure regulatory compliance and data integrity. Responsibilities include site initiation and management, verifying informed consent, and documenting activities. The ideal candidate will have a Bachelor's degree or RN, knowledge of Good Clinical Practice, and strong communication skills. The position may require travel up to 75%.