Description
The Clinical Research Administrator will support clinical research projects by maintaining databases, tracking systems, and large volumes of documents; serving as the primary communication point for investigative sites and internal departments; coordinating site-specific query resolution, training, and system access; preparing meeting agendas and minutes; and handling correspondence and calls. The role requires a Life Sciences college or university degree, Polish and English proficiency, MS Office proficiency, and strong organizational, planning, and problem-solving skills; prior clinical research or CRO administrative experience is preferred. Benefits include a permanent work agreement, competitive salary, flexible working hours, life and medical insurance, and additional days off.
