Site Monitoring CRA – Junior to Senior

ImmigrationGPT; Manchester; Hybrid; GBP 35,000 - 43,000; Full time

Job summary

IQVIA UK's Site Management team in Manchester is expanding, seeking junior and experienced Clinical Research Associates to support multi-sponsor trials.

You will perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH guidelines and regulatory requirements, contributing to timely, high-quality trial delivery.

This role offers a clear career path in a global CRO environment with robust training and ongoing professional development.

Qualifications

• Experience as Clinical Research Associate or junior CRA.
• Knowledge of GCP/ICH guidelines.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Skills

GCP knowledge

ICH guidelines

Site monitoring

Job description

IQVIA UK's Site Management team in Manchester is expanding, seeking junior and experienced Clinical Research Associates to support multi-sponsor trials.

You will perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH guidelines and regulatory requirements, contributing to timely, high-quality trial delivery.

This role offers a clear career path in a global CRO environment with robust training and ongoing professional development.