Clinical Research Associate

What You Will Do

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
• Key Responsibilities Include:
• 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.

Your Profile

• You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
• Required Qualifications And Experience:
• 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%).

What ICON Can Offer You

• Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
• Examples Include:
• Variety of annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

About the Role

• Georgia ICON plc is a world-leading healthcare intelligence and clinical research organization.
• We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
• This position is sponsor dedicated supporting our client monitoring cardio and obesity trials.
• Must be located in Georgia.

Benefits

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

Equal Opportunity Employer

ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Contact Information

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply.