Senior CRA
About The Position
At ICON Strategic Solutions, the Senior Clinical Research Associate (CRA) works in a sponsor-dedicated model, supported by ICON’s global expertise. The role leads clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. The position focuses on ophthalmology and requires candidates to be located in the greater Chicago area, with approximately 60% travel as required. The CRA monitors clinical trial sites for compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards; conducts site visits to assess performance, resolve issues, and support successful trial execution; and works with cross-functional teams to ensure timely, accurate data collection and reporting. The role also provides training and guidance to site staff and other CRAs and builds effective relationships with site personnel and stakeholders. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. ICON is an equal opportunity employer committed to an inclusive and accessible workplace and can provide reasonable accommodations during recruitment upon request.
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Experience monitoring complex indications in Ophthalmology.
- Willingness to travel as required (approximately 60%).
- Must be located in the greater Chicago area.
- Must have the legal right to work in the country where the role is based.
Responsibilities
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and support successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
- Lead clinical trial monitoring tasks requiring technical depth, focusing on quality and continuous improvement.
Benefits
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
