Clinical Research Nurse Bełchatów
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Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
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.
#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
The potential base pay range for this role when annualized is zł102800.00 - zł190900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.Required Experience:
IC
Key Skills
- Clinical Research
- FDA Regulations
- Data Collection
- GCP
- Infusion Experience
- Phlebotomy
- Clinical Trials
- Pediatrics Experience
- Qualitative Research Interviewing
- Research Experience
- Nursing
- Epic
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
