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 researchStrong communication skills and fluency in English.Proficient in MS Office and clinical trial systems.