Working in compliance means every day is different. The one day you are developing processes, the other you are creating a tool or a training-program for CRA’s. Whether you are creating a monitoring manual, organizing an investigator meeting, answering questions about last week’s training program or training CRA’s; one thing is for sure, you are constantly interacting with people in- and outside our organization. You will deal with different stakeholders throughout the organization and will answer questions from every corner of our organization. You will work at the same time on different (international) clinical trials, in different therapeutic areas and in different phases. Each study requires its own approach, which makes the job very interesting and challenging.
As PCM you will ensure compliance with the Julius Clinical quality requirements and standards by providing compliance management of clinical trial processes, tools, reports and systems across assigned trials. The job asks you to perform in a calm and collected way during demanding, challenging circumstances.