Site Manager (clinical research, local site coordinator role)

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put on patient related site support, with the aim to maximise the utilisation of site staff designated to a given study (e.g. study site coordinator, study nurse, sub-investigator) through provision of site training and oversight for logistically / technically more demanding study procedures. The SM is working under the supervision of Senior SM or Director of Site Management (or LSM on project level).

Role and Responsibilities:

Conducts patient related site support as per study specific site management plan

Ensures the progress of the clinical study and that it is conducted, recorded, and reported in accordance with the protocol, Ergomed standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s)