Clinical Research Associate II, Oncology

IQVIA

Clinical Research Associate II performing site monitoring of interventional studies in the UK. Ensuring compliance with GCP and ICH guidelines while maintaining effective collaboration with sites.

Posted 4/16/2026full-timeManchester • 🇬🇧 United KingdomJuniorMid-LevelWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
Evaluate the quality and integrity of study site practices and manage the progress of assigned studies.

Requirements

What you’ll need

At least 1 year of independent on-site monitoring experience of interventional studies in the UK.
Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
Good therapeutic and protocol knowledge as provided in company training.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Benefits

Comp & perks

Professional development opportunities
Flexible working hours

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

site monitoringinterventional studiesclinical researchGood Clinical Practice (GCP)International Conference on Harmonization (ICH) guidelinesprotocol knowledge

Soft Skills

effective working relationshipscommunication