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

Location: Plzeň/Pilsen, Czech Republic; Prague, Czech Republic

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.

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.