Clinical Research Nurse

Clinical Research Nurse / Clinical Research Coordinator - Bełchatów part time 20-24h per week

Start Date: immediately, asap

Duration: Approximately 5 months

IQVIA is currently recruiting a dedicated Clinical Research Nurse / Clinical Research Coordinator to support a clinical research site in Bełchatów. 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
• Take and record vital signs (incl. weight, height), perform ECG
• Patient communication, screening and enrollment, including handling informed consent and privacy documentation
• Handling patient referrals and communication with referring Doctors/Specialists
• Investigational Product (IP): Manage receipt and storage, perform accountability and compliance, prepare, dispense and administer IP
• 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:

• Current RN registration
• 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 2-3 years experience working as a Research Nurse at a clinical trial site
• Experience in collecting patient vital signs and laboratory samples, administering investigational products, and conducting electrocardiograms (EKGs)
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail

Clinical Research Nurse / Clinical Research Coordinator - Bełchatów part time 20-24h per week

Start Date: immediately, asap

Duration: Approximately 5 months

IQVIA is currently recruiting a dedicated Clinical Research Nurse / Clinical Research Coordinator to support a clinical research site in Bełchatów. 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
• Take and record vital signs (incl. weight, height), perform ECG
• Patient communication, screening and enrollment, including handling informed consent and privacy documentation
• Handling patient referrals and communication with referring Doctors/Specialists
• Investigational Product (IP): Manage receipt and storage, perform accountability and compliance, prepare, dispense and administer IP
• 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:

• Current RN registration
• 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 2-3 years experience working as a Research Nurse at a clinical trial site
• Experience in collecting patient vital signs and laboratory samples, administering investigational products, and conducting electrocardiograms (EKGs)
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail

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.