FAQs
What is the primary focus of the IQVIA Research and Development Solutions team?
The primary focus is to help healthcare customers find innovative treatment solutions for patients with various illnesses, whether common, large, or rare.
What are the main responsibilities of the Clinical Trials Assistant?
The main responsibilities include assisting Clinical Research Associates (CRAs) and the Regulatory and Start-Up (RSU) team with updating clinical systems, preparing and managing clinical documentation, handling Clinical Trial Supplies, acting as a central contact for project communications, and performing assigned administrative tasks.
What educational qualifications are required for this position?
A high school diploma/certificate or the country’s educational equivalent along with 3 years of administrative support experience is required.
What languages are necessary for this role?
Good written and verbal communication skills in both English and French are necessary.
What computer skills are expected from the Clinical Trials Assistant?
Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook is expected.
Where is the position located?
The position is office-based in La Défense, France.
What type of skills are important for this role?
Effective time management, organizational skills, and the ability to establish and maintain effective working relationships with coworkers, managers, and customers are important.
What type 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, focused on accelerating the development and commercialization of innovative medical treatments.