- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess performance, resolve issues, and provide support for 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.
- Ensure compliance with all relevant regulations, guidelines, and company policies.
Job Requirements
- Advanced degree in life sciences, nursing, or medicine.
- Minimum 3-6 years of 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, demonstrating 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 and ability to travel across the country as required by the role.
Perks and Benefits
- Competitive salary and benefits package.
- Opportunity to work with a leading healthcare intelligence and clinical research organization.
- Inclusive environment fostering innovation and excellence.
- Flexible working hours and remote work options available.
- Comprehensive training and development programs offered.
- Global Employee Assistance Programme, LifeWorks, providing 24-hour access to a global network of over 80,000 independent specialized professionals for employee and family 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 Company
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development through innovative solutions and services. We foster an inclusive environment that embraces diversity and promotes excellence, and we welcome candidates who share our values and passion for delivering exceptional results.
At ICON, inclusion & belonging are fundamental to our culture and values. Were 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. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply.
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