Clinical Research Coordinator

You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

• Assisting in the planning, initiation, and execution of clinical trial activities
• Conducting site feasibility assessments and participating in site selection processes
• Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
• Monitoring study progress and data collection activities to ensure quality and accuracy
• Assisting in the preparation and review of study documentation and reports

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a relevant field, such as life sciences or healthcare
• Previous experience in clinical research or a related field preferred
• Strong organizational and communication skills
• Ability to work independently and collaboratively in a fast-paced environment
• Attention to detail and ability to prioritize tasks effectively

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.