Sr. Clinical Trial Assistant

IQVIA, Inc.; Reading; Hybrid; GBP 25,000 - 35,000; Full time

Job summary

A leading global provider of clinical research services is seeking a Clinical Trial Assistant in Reading. This role involves supporting the clinical team in document management, maintaining accurate records, and ensuring compliance with clinical guidelines. The position offers hybrid working options from specific UK locations and may consider fully remote arrangements for certain projects.

Qualifications

• Minimum 8-16 months of clinical trial assistance experience.
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines preferred.
• Good command of English language and effective communication skills.

Responsibilities

• Assist with updating and maintaining clinical documents and systems.
• Manage and track Case Report Forms (CRFs) and clinical data flow.
• Act as a central contact for project communications.

Skills

Communication

Time Management

Organizational Skills

Education

Life science degree or equivalent industry experience

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Internal Job Description

IQVIA are seeking a Clinical Trial Assistant to join us on our mission to drive healthcare forward. Hybrid working available from either Luton or High Wycombe offices (2-3 days per week), depending on your location and business needs. A fully remote contract may be considered for specific projects.

Sr. Clinical Trial Assistant will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

*Please note - this role is not eligible for UK visa sponsorship*

Essential Functions

• Assist Clinical Research Associates and Regulatory and Start-Up team with updating and maintaining clinical documents and systems (e.g., Trial Master File)
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Qualifications / Experience

• Minimum 8-16 months of clinical trial assistance experience
• Life science degree educated or equivalent industry experience.
• Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines preferred.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com