FAQs
What is the location of the Clinical Research Coordinator / Study Nurse position?
The position is located in Giessen.
What is the duration of the employment for this position?
The employment is for approximately 6-12 months.
What are the main responsibilities of the Clinical Research Coordinator / Study Nurse?
Responsibilities include coordinating clinical research studies, ensuring patient well-being, maintaining study documents, planning logistical activities for study procedures, and supporting patient recruitment.
What qualifications are required for this role?
Candidates should have at least two years of relevant experience or an equivalent combination of medical education, training, and experience.
Are there specific IT skills required for this job?
Yes, candidates should have strong IT skills and be proficient in MS Windows and Office applications such as Access, Outlook, Excel, and Word.
Is knowledge of clinical studies necessary for this role?
Yes, a solid understanding of clinical studies, including relevant workflows, consent forms, and study protocols, is required.
What language skills are necessary for this position?
Candidates must have very good German language skills, both spoken and written.
Who will the Clinical Research Coordinator / Study Nurse report to?
The role will operate under the direction and delegation of the Principal Investigator.
What kind of company is IQVIA?
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
When is the expected start date for this position?
The position has a start date as soon as possible.