Clinical Research Associate

The opportunity to join on a 12 month contract as a CRA supporting a global pharma company in delivery of neurology and digital clinical trials. Onsite and remote working required.

Key Responsibilities :

Provide operational support for remote patient monitoring solutions and act as a key point of contact for study teams and sites.

Support the preparation and submission of IRB / Ethics Committee documentation and responses.

Maintain accurate study progress tracking and data overviews across recruitment, data transfer, and issue resolution.

Requirements :

Several years’ experience in clinical research

Strong communication skills and fluency in English.

Proficient in MS Office and clinical trial systems.