FAQs
What is the job title for this position?
The job title is Clinical Trial Assistant.
What company is offering this position?
The position is offered by IQVIA cFSP.
What is the main responsibility of the Clinical Trial Assistant?
The main responsibility is to perform daily administrative activities to ensure a complete and accurate Trial Master File delivery in collaboration with Clinical Research Associates and Regulatory and Start-Up teams.
Is this position fully remote?
No, while remote working is allowed, on-site work is required on an ad-hoc basis in Buckinghamshire.
What educational background is required for this position?
A life science degree or equivalent industry experience is required.
How much clinical trials experience is ideally needed for this role?
Ideally, 6-12 months of clinical trials experience is needed.
Are there specific guidelines that the candidate should be familiar with?
Yes, knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is preferred.
What computer skills are necessary for the Clinical Trial Assistant position?
Proficiency in Microsoft Word, Excel, and PowerPoint is necessary.
What kind of communication skills are required for this role?
Effective written and verbal communication skills, along with a good command of the English language, are required.
Do we provide visa sponsorship for this role?
No, this role is not eligible for UK visa sponsorship.
What are the key organizational skills required for this position?
Effective time management and organizational skills are key requirements.
Who does the Clinical Trial Assistant collaborate with?
The Clinical Trial Assistant collaborates with Clinical Research Associates (CRAs) and Regulatory and Start-Up teams.
Is this position focused on patient interaction?
No, the role is primarily administrative and does not involve direct patient interaction.
How can I learn more about the company and its services?
You can learn more at the IQVIA careers website at https://jobs.iqvia.com.