FAQs
What is the job title for this position?
The job title for this position is Clinical Research Coordinator / Study Nurse (m/w/d) - Krefeld.
What are the primary responsibilities of this role?
The primary responsibilities include coordinating clinical research studies, ensuring patient well-being, maintaining study documentation, planning logistical activities, data entry, and supporting patient recruitment.
How many hours per week is this position?
This position is part-time, requiring 20 hours per week.
What is the duration of this position?
The position is for approximately 5 months.
Are there any specific experience requirements for this role?
Yes, candidates should have at least two years of relevant experience or an equivalent combination of medical education, training, and experience.
What technical skills are required for this job?
Candidates should have strong IT skills and be proficient in MS Windows and Office applications such as Access, Outlook, Excel, and Word.
What language skills are necessary for this role?
Very good German language skills, both spoken and written, are required.
Who will be supervising the Clinical Research Coordinator / Study Nurse?
The role will operate under the leadership and delegation of the Principal Investigator.
What kind of company is IQVIA?
IQVIA is a leading global provider of clinical research services and healthcare intelligence, focusing on improving patient outcomes and population health worldwide.
When is the expected start date for this position?
The position is available to start immediately.