Clinical Trials Assistant Review
at NHS
Placement (10 Months+)
Research
Manchester
Review Submitted: October 2025
Overall Rating
5 /5
The Overall Rating is the average of all the ratings given in each category. We take those individual ratings and combine them into one final score!
Overview of Role
Please give an overview of your role and what this involves on a day-to-day basis.
• Maintaining Trial Documentation: Preparing and updating essential study documents, including Investigator Site Files (ISFs), delegation logs, screening logs, and enrolment trackers.
• Data Entry and Database Management: Inputting clinical and laboratory data into electronic data capture (EDC) systems such as RedCap or sponsor-specific platforms, ensuring accuracy and timely query resolution.
• Supporting Patient Visits: Assisting Clinical Trials Coordinators and Research Nurses with pre- and post-visit preparations, such as printing patient notes, booking appointments, organising sample collection forms, and handling trial packs.
• Liaising with Internal and External Teams: Communicating with pharmacy, pathology, radiology, and trial sponsors to coordinate aspects such as drug accountability, sample shipments, and monitoring visits.
• Sample Processing and Logistics: Completing sample request forms, packaging biological samples according to protocol, and arranging courier collections.
• General Administrative Support: Managing shared inboxes, tracking patient reimbursements, organising study meetings, and contributing to site file audits or monitoring visits.