FAQs
What is the job title for this position?
The job title is Clinical Research Coordinator.
Where is the job location?
The job is located in Verona, supporting a site in Florence.
What is the duration of the position?
The position is expected to last approximately 13 weeks.
How many hours per week is the job?
The job is for 24 hours per week.
What are the main responsibilities of the Clinical Research Coordinator?
The main responsibilities include maintaining study documents, supporting patient screening and enrollment, coordinating study procedures, data entry and quality checking, managing biological samples, coordinating with study monitors, and performing administrative research tasks.
What qualifications are required for the position?
Candidates should have a BS/BA in life sciences or equivalent work experience in a clinical environment, good knowledge of clinical trials, basic knowledge of medical terminology, strong IT skills, excellent interpersonal and organizational skills, and be fluent in Italian with good English language skills.
Is experience in a clinical environment necessary?
Yes, relevant work experience in a clinical environment or medical setting is required.
What software skills are preferred for this job?
Strong IT competence, including proficiency in MS Windows and Office applications like Access, Outlook, Excel, and Word, is preferred.
Is knowledge of clinical trials important for this role?
Yes, a good knowledge of clinical trials and departmental operating procedures is important for this role.
How can I apply for this position?
If this opportunity sounds perfect for you, please apply now through the provided application channels.
Who is the employer for this position?
The employer is IQVIA, a leading global provider of clinical research services.