Clinical Trial Assistant

IQVIA Argentina; Manchester; Hybrid; GBP 24,000 - 32,000; Full time

Benefits offered by this job

Office-based role

Career development opportunities

Exposure to clinical trials

Job summary

IQVIA is seeking a Clinical Trial Assistant for the Medicines Evaluation Unit (MEU) to support CRAs and RSU in TMF maintenance and document management within a hospital-based research facility. The role emphasizes accuracy, organization and timely document handling.

Requirements include a High School Diploma, 2–3 years relevant experience and strong English communication. The position offers an office-based work environment with opportunities across therapeutic areas and career progression.

Qualifications

• Good command of English (written and spoken).
• Experience with trial master file (TMF) systems is beneficial.
• Proven ability to handle multiple tasks in a regulated environment.

Responsibilities

• Assist CRAs and RSU with updating and maintaining TMF and related documents.
• Prepare, handle, file and archive clinical documentation and reports per procedures.
• Assist with preparation and distribution of Clinical Trial Supplies and track CRFs and data flow.
• Serve as central contact for project communications and documentation.
• Perform daily administrative tasks to ensure accurate TMF delivery.

Skills

Communication skills

MS Word

MS Excel

MS PowerPoint

Clinical research experience

Education

High School Diploma

2–3 years relevant experience

Job description

Clinical Trial Assistant

Medicines Evaluation Unit (MEU)

This role is office based!

The Medicines Evaluation Unit (MEU) Ltd, an IQVIA business, is one of the UK’s leading contract research organisations, and a facility where commitment to excellence is paramount. Possessing extensive pharmaceutical, scientific and clinical expertise, allied with fast volunteer recruitment, both healthy and patient, within a state-of-the-art hospital based research facility, enables the MEU to offer clients positive clinical trial solutions.

Join us on our exciting journey!

Job Overview:

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.

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 CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate 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.

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.

Requirements:

• High School Diploma or equivalent
• 2-3 years of relevant experience.
• Must have commercial experience.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Clinical research experience preferred.

Join IQVIA to see where your skills can take you

• High level of autonomy.
• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.