Responsibilities;
-Ensure adherence to SOPs, regulations and ICH-GCP
-Perform monitoring visits from 8 - 10 per month
-Liaising with medical staff on-site and principal investigators
-Track patient recruitment by keeping in contact with investigators
-Identifying, evaluating and organising documentation ready for submissions to ethics committees
-Performing site initiation and closeout visits

Requirements;
-2+ Years independent monitoring experience
-Life science or similar field Bsc University qualification
-Effective communication, planning and organisation skills
-Ability to learn new SOPs
-Good understanding and competency of basic computer systems
-ICH-GCP, EU and FDA understanding