Description
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.