FAQs
What is the location requirement for this position?
This role requires frequent travel to Luton.
What type of company is IQVIA?
IQVIA is a leading global provider of contract research services, advanced analytics, and technology solutions to the life sciences industry.
What educational background is needed for this position?
While the job description does not specify a required educational background, a background or knowledge in clinical research or life sciences is typically beneficial.
What are the primary responsibilities of a Clinical Trial Assistant?
The primary responsibilities include assisting Clinical Research Associates with clinical documentation, tracking site compliance, managing clinical trial supplies, and supporting project communications.
Is prior experience in clinical research necessary for this role?
While prior experience in clinical research is not explicitly stated, awareness of clinical research regulatory requirements and knowledge of Good Clinical Practice are important.
What skills are essential for this role?
Essential skills include good written and verbal communication, effective time management, organizational skills, and proficiency in Microsoft Word, Excel, and PowerPoint.
Is this position eligible for UK visa sponsorship?
No, this role is not eligible for UK visa sponsorship.
What does IQVIA value in terms of workplace culture?
IQVIA strongly advocates for diversity and inclusion, believing that an inclusive workplace fosters a sense of belonging and enhances team strength.
Will there be opportunities for professional development?
Yes, IQVIA provides access to world-class training and professional development opportunities.
Can Clinical Trial Assistants accompany CRAs on site visits?
Yes, Clinical Trial Assistants may accompany CRAs on site visits to assist with clinical monitoring duties after completing required training and obtaining necessary approval.