Experienced CRA - Single Sponsor Dedicated

IQVIA · Berkshire, UK

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks experienced Clinical Research Associates for sponsor-dedicated roles in Reading, Berkshire. Candidates will conduct site monitoring activities, manage subject recruitment, and ensure protocol compliance across multiple investigative sites in accordance with GCP and ICH guidelines.

What they're looking for

Minimum 6 months of independent on-site monitoring experience
Successful management of multiple clinical trial protocols at diverse sites
In-depth knowledge of GCP and ICH guidelines
Life science degree or equivalent industry experience
Willingness to travel to trial sites

What you'll be doing

Conduct site monitoring visits including selection, initiation, ongoing monitoring, and close-out activities
Develop and track subject recruitment plans aligned with study objectives
Deliver protocol training and maintain regular site communication
Assess quality and integrity of site practices and escalate compliance issues
Manage study progress tracking, documentation filing, and regulatory submissions

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Date posted16 days ago

Last source check1 day ago

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