Clinical Research Coordinator (Part-Time, Mariánské Lázně)

About the role

IQVIA is recruiting a Site Research Assistant / Clinical Research Coordinator for a clinical research site in Mariánské Lázně. The position is part-time, about 18 hours per week, with an immediate start and a duration of approximately six months. You will help ensure the smooth execution of the clinical trial through administrative and clinical support tasks.

Key responsibilities

• Maintain and update study documentation, including protocols, case report forms (CRFs) and Electronic Data Capture (EDC) systems
• Support patient screening and enrollment, including informed consent and privacy documentation
• Coordinate logistical activities for study procedures in line with the protocol
• Enter data, perform quality checks and resolve queries to ensure data accuracy and completeness
• Manage and ship biological samples
• Communicate with study monitors and respond to study-related inquiries
• Carry out general administrative tasks related to the study

Required profile

• Bachelor's degree in life sciences or equivalent education, and/or relevant experience in a clinical or medical setting (e.g. clinical research coordinator, research assistant, nurse, medical assistant)
• Solid understanding of clinical trials and familiarity with study protocols, consent forms and schedules
• Good knowledge of medical terminology
• At least 1-2 years of experience as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
• Fluency in Czech and good command of English

Required skills

• Proficiency in MS Office applications (Outlook, Word, Excel, Access)
• Good interpersonal and communication skills
• Strong organisational skills and attention to detail