Key responsibilities include:

• Coordinating and managing the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics.
• Ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial.
• Monitoring and documenting trial progress, including data collection, safety reporting, and regulatory compliance.
• Providing training and support to site staff to ensure the effective execution of trial procedures and protocols.
• Building and maintaining strong relationships with study participants and site personnel to facilitate smooth trial operations and address any issues that arise.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Coordinator, with a comprehensive understanding of clinical trial processes and regulatory requirements.
• Strong organisational and multitasking skills, with the ability to manage multiple aspects of clinical trials simultaneously.
• Proficiency in clinical trial software and tools, with a keen eye for detail and accuracy in data management and documentation.
• Excellent communication, interpersonal, and problem-solving skills, with the ability to work effectively with a diverse team and drive successful trial outcomes.

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Job Data by YubHub.