IQVIA

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

In short

This is a part-time, 6-month Clinical Research Coordinator / Site Research Assistant role supporting a clinical trial site in Mariánské Lázně, Czech Republic, requiring 2 on-site days per week with travel from anywhere in the Czech Republic. The role involves maintaining study documentation, supporting patient screening and consent, data entry and query resolution, and managing biological samples at a clinical research site. IQVIA, a global clinical research and healthcare intelligence provider, is hiring. Candidates need 1-2 years of clinical research coordination experience, a life sciences degree or equivalent, and fluency in Czech plus good English.

Travel Site Research Assistant / Clinical Research Coordinator – Czech Republic (Part-Time, 2 Days per Week)
Location: Mariánské Lázně, Czech Republic – Travel required
Start Date: Immediate
Duration: Approximately 6 months
Working Schedule: 2 days per week
IQVIA is currently recruiting a dedicated Site Research Assistant / Clinical Research Coordinator to support a clinical research site in Mariánské Lázně.
The opportunity is open to candidates from across the Czech Republic who are willing to travel to the site. The position is planned for 2 on-site days per week, which may be arranged as consecutive days. An overnight stay may also be considered if required.
Key Responsibilities
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
Your Profile
•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
The Opportunity
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.
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.

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