Clinical Study Manager Medical Devices
Whether you are at home or in the office or at a customer, the moment you open your laptop the sponsor questions and site queries in your inbox have your direct attention.
What makes your day as a Clinical Study Manager diverse and challenging is that you manage two to four clinical projects for our customers at the same time. Where one project is in the phase of answering questions from the Ethics Committee, on another project the CRA expects her monitoring report reviewed in return before noon.
In the morning you have a meeting scheduled with the other Clinical Study Managers to discuss each other’s studies and help each other out with any issues. Also, you have a kick-off call with a new client, whereas you are halfway finishing a monitoring report for another client. In the (international) dynamics of your job, you plan the afternoon free for completing some administrative tasks before you set out travelling to a site selection visit to Germany.
Does this sound like your new job? Then Qserve’s CRO, a growing organization with a lot of freedom and also a high level of exposure and steep learning curve, is looking for you:
A Mid-career CRA / Junior Clinical Study Manager with an affinity for medical devices.