Monitoring practices jobs

Senior CRA

ICON plc · Posted Nov 9, 2026

Copenhagen, Capital Region, Denmark
Senior

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Senior Clinical Research Associate overseeing and managing clinical trial activities to ensure compliance with protocols, regulatory requirements, and industry standards.

Responsibilities

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Requirements

Advanced degree in a relevant field such as life sciences, nursing, or medicine

Skills

monitoring practices data integrity site management Good Clinical Practice (GCP)clinical trial software

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Senior CRA

Responsibilities

Requirements

Skills

Benefits