Clinical Research Coordinator - Mariánské Lázně
IQVIA
Plzeň/Pilsen, Czech RepublicPosted 4 days agoDiscoveredMatch locked
Part time1+ years exp
Site Research Assistant / Clinical Research Coordinator – Mariánské Lázně (Part-Time, 18 hours per week)
Start Date
: Immediate
Duration
: Approximately 6 month
IQVIA is currently recruiting a dedicated Site Research Assistant /Clinical Research Coordinator to support a clinical research site in Mariánské Lázně. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical 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
We are looking for candidates who bring a combination of education, experience, and skills:
- 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
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
- Excellent interpersonal and communication skills
- Strong organizational skills and attention to detail
- Fluency in
Czech
and good command of English
Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.
Interested?
If this sounds like the right opportunity for you, we encourage you to apply today.
#LI-HCPN
#LI-CES
#LI-DNP
#LI-NS1
#LI-Onsite
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.
Not included in the source posting: about the role, qualifications.
Skills
excel
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.