Senior CRA

ICON Strategic Solutions; Georgia; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme (LifeWor

Life assurance

Flexible country-specific benefits

Job summary

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.

Senior CRA position in the United States (Georgia) focusing on leading clinical trial monitoring tasks with emphasis on quality and continuous improvement.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management with proficiency in relevant software and tools.
• Excellent communication, interpersonal, and stakeholder management skills with ability to influence and drive compliance.

Responsibilities

• Leading clinical trial monitoring tasks with depth and focus on quality and continuous improvement.
• Monitoring sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Conducting site visits to assess performance, resolve issues, and support trial execution.
• Collaborating with cross-functional teams to ensure timely data collection and reporting.
• Providing training and guidance to site staff to maintain high standards of trial conduct.
• Building and maintaining relationships with site personnel and stakeholders for smooth operations.

Skills

Clinical trial monitoring

Site management

Data integrity

Communication skills

Stakeholder management

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline

Tools

Clinical trial software

Job description

Senior CRA

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.

What You Will Do

You will lead clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key Responsibilities Include

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.

Required Qualifications And Experience

• 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.
• Willingness to travel as required (approximately 60%).

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include

• Various 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, subsidised travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. 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.

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.