Travel Site Research Assistant / Clinical Research Coordinator – Czech Republic (2 days per week))

As a key member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical research support tasks, including:

• →Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
• →Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• →Coordinating logistical activities for study procedures in line with the study protocol
• →Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
• →Managing and shipping biological samples
• →Communicating with study monitors and responding to study-related inquiries
• →Carrying out general administrative tasks related to the study

• Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting
• At least 1–2 years of experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
• Solid understanding of clinical trials and familiarity with study protocols, informed consent forms and study schedules
• Good knowledge of medical terminology
• Strong IT skills, including proficiency in MS Office applications
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail
• Fluency in Czech and a good command of English
• Willingness to travel to Mariánské Lázně for 2 on-site days per week

This is a part-time assignment for approximately 6 months, offering the opportunity to work directly with a clinical research site and contribute to the successful delivery of a clinical trial.

Candidates from across the Czech Republic who are open to a travel-based setup are encouraged to apply.

Interested?
If this sounds like the right opportunity for you, we encourage you to apply today.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.