Senior Clinical Research Associate - Frontline Trials (UK)

IQVIA

Reading

On-site

GBP 35,000 - 52,000

Full time

3 days ago

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Job summary

IQVIA is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring and drive study execution across selected sites. This role requires strong GCP/ICH knowledge, a life science background, and travel to various sites.

The position offers opportunities to work with cutting-edge medicines and contribute to pivotal clinical research efforts within a global organization. You'll collaborate with cross-functional teams to ensure quality and compliance throughout the trial

Qualifications

Minimum 6 months of independent on-site monitoring experience.
Experience managing multiple clinical trial protocols across diverse sites.
Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines.
Bachelor's degree in life sciences or equivalent industry experience.
Willingness to travel to sites as needed.

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope and GCP/ICH requirements.
Collaborate with sites to drive subject recruitment plans for project needs.
Provide protocol training to sites and maintain regular communication on study outcomes.
Assess site practices and escalate quality issues following regulatory standards.
Track regulatory submissions, recruitment, CRFs, and data queries; support startup activities as needed.
Ensure TMF/ISF documents are filed and maintained per requirements.
Create reports and follow-up communications documenting visit findings and actions.
Liaise with the study team to support project execution.