Impress employers and recruiters.
Choose from hundreds of resume examples.
Impress employers and recruiters.
Choose from hundreds of resume examples.
Tailor your resume to this CTC role.
Rezi rewrites your resume against ICON plc's job description. Free.
Tailor your resume to this CTC role.
Rezi rewrites your resume against ICON plc's job description. Free.
Don't guess if your resume is good enough.
See how it scores against the CTC posting at ICON plc — free, in seconds.
Don't guess if your resume is good enough.
See how it scores against the CTC posting at ICON plc — free, in seconds.
About the Role
As a Clinical Trial Assistant (CTA) at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency. You will work in a sponsor-dedicated model, supported by ICON’s global expertise.
Responsibilities
- Assist in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Support site management activities, including documentation preparation, data entry, and tracking site performance metrics.
- Collaborate with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintain accurate records of site activities and contribute to the preparation of monitoring reports.
- Participate in training and development initiatives to enhance knowledge and skills in clinical trial management.
Requirements
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
- Basic knowledge of clinical trial processes and regulatory requirements is a plus.
- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.
- Willingness to travel as required (approximately 25%).
- Must have the legal right to work in the country where the role is based.
Skills
- Organizational skills
- Attention to detail
- Communication skills
- Interpersonal skills
Location
- Australia, Sydney
Work Type
- Hybrid
- Full-time
Experience Level
- Entry-level
Education Level
- Bachelor's degree
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
About the Company
- ICON is the world’s largest FSP organisation, with over 90 sponsor partnerships.
- We offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
Equal Opportunity
- ICON is an equal opportunity employer.
- We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
- If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.