Study Coordinator/CRA

We are looking for a Study Coordinator / Site Coordinator with 1–4 years of hands-on site experience, who is motivated to progress into a CRA role.

It is an advantage if you have already been exposed to basic monitoring tasks, or if you are clearly aiming to develop toward CRA responsibilities.

Responsibilities:

• support pre-trial preparation and collection of required study documentation
• assist with ethics committee submissions and coordination of regulatory documents
• manage and maintain the Investigator Site File (ISF) and other site-level study files
• collaborate with investigators, study nurses and other site staff in day-to-day study activities
• support patient screening and visit preparation according to protocol
• handle sample management and logistics (lab kits, shipments, related documentation)
• ensure availability and proper maintenance of study supplies and materials
• support training of site staff on study-specific procedures
• perform selected basic monitoring tasks under supervision (e.g., partial SDV)
• liaise with CRA colleagues and provide site-level insights
• support EDC data entry, query resolution and general study documentation
• assist in site close-out activities at the end of the trial

Requirements:

• proven Study Coordinator / Clinical Research Coordinator (CRC) experience – site-level background is essential
• good understanding of GCP and clinical trial processes
• strong organisational skills and attention to detail
• clear motivation to progress into a CRA career path
• strong communication skills with investigators and clinical site teams