Respiratory Clinical Trial Technician – Entry Level

IQVIA; Manchester; On-site; GBP 26,000 - 34,000; Full time

Benefits offered by this job

High autonomy

Global exposure

Therapeutic variety

Collaborative team

In-house technology

Career progression

Work-life balance

Job summary

IQVIA's Medicines Evaluation Unit (MEU) in Manchester seeks a Clinical Trial Technician. The role focuses on conducting physiological tests and supporting the setup and management of clinical studies in a state-of-the-art hospital research facility.

Full-time training is provided and there is a strong emphasis on clinical data integrity and patient safety. You will work on respiratory and related therapeutic areas, coordinating with sponsors and sites, while developing skills in ARTP‑recognized

Qualifications

• Bachelor's degree in a scientific discipline required or desirable.
• Interest in developing skills in clinical physiology and respiratory science.
• Microsoft Word, Excel and PowerPoint proficiency.

Responsibilities

• Perform complex clinical procedures on subjects, incl. spirometry.
• Conduct bronchodilator and challenge testing, oscillometry, DLCO and related measures.
• Collect, record and report data per the protocol and SOPs.
• Support Phase I–IV studies, ensuring adherence to protocol and GCP.
• Maintain and update skills per ARTP guidelines.
• Participate in study setup, management, and data reconciliation with third parties.
• Contribute to study training activities and audits/regulatory inspections.
• Support a broad range of therapeutic areas including respiratory and others.

Skills

Microsoft Word

Microsoft Excel

PowerPoint

Education

Bachelor's Degree in Scientific Discipline

Job description

IQVIA's Medicines Evaluation Unit (MEU) in Manchester seeks a Clinical Trial Technician. The role focuses on conducting physiological tests and supporting the setup and management of clinical studies in a state-of-the-art hospital research facility.

Full-time training is provided and there is a strong emphasis on clinical data integrity and patient safety. You will work on respiratory and related therapeutic areas, coordinating with sponsors and sites, while developing skills in ARTP‑recognized