Clinical Trial Assistant TMF & Data Coordinator

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

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.