Physical Therapist to Clinical Research Associate (CRA)

ICON Strategic Solutions is a clinical research organization supporting sponsor-dedicated clinical development programs. The Clinical Research Associate role is responsible for monitoring clinical trials, ensuring protocol compliance and data integrity, collaborating with research sites, and maintaining high-quality study documentation.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborating with investigators and site staff to facilitate smooth study conduct
• Performing data review and resolution of queries to maintain high-quality clinical data
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Benefits

• 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

Company

• Outsourced clinical development and commercialization services for life sciences
• Dublin , GB
• https://www.iconplc.com/services/strategic-solutions/
• 10001+ employees

Qualifications

• Travel of approximately 50% is required
• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills, with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness to travel as required (approximately 60%)
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based
• Minimum of 2 years of experience as a Clinical Research Associate.

Required skills

• Clinical Trial Monitoring, Clinical Trial Processes, Clinical Trial Regulations, ICH-GCP Guidelines, Independent and Collaborative Work, Protocol Compliance

Experience

• 2+ years