Clinical Research Associate

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Execute site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Maintain protocol adherence, data integrity, and patient safety throughout the trial phases.

• Collaborate with investigators and site personnel to ensure smooth execution of the study.

• Conduct data reviews and resolve queries to uphold the quality of clinical data.

• Assist in the preparation and evaluation of study documentation, which includes protocols and clinical study reports.

• Operate within a sponsor-dedicated framework backed by ICON’s global expertise.

• Design and analyze clinical trials, interpret intricate medical data, and contribute to innovative treatment and therapy development.

⛳️ Requirements

• A Bachelor’s degree in a scientific or healthcare-related discipline.

• A minimum of 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen attention to detail.

• Capacity to work both independently and as part of a team in a dynamic environment.

• Willingness to travel as necessary (approximately 60%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.