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 CRA II role.
Rezi rewrites your resume against ICON plc's job description. Free.
Tailor your resume to this CRA II 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 CRA II posting at ICON plc — free, in seconds.
Don't guess if your resume is good enough.
See how it scores against the CRA II posting at ICON plc — free, in seconds.
About the Role
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. You will work in a sponsor-dedicated model, supported by ICON’s global expertise. As 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.
Responsibilities
- Contribute to clinical trial monitoring activities, taking responsibility for deliverables and working collaboratively.
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Requirements
- 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%).
- Must have the legal right to work in the country where the role is based.
Skills
- Clinical trial monitoring
- Protocol compliance
- Data integrity
- Patient safety
- Data review
- Query resolution
- Study documentation preparation
- Organizational skills
- Communication skills
- Attention to detail
Location
- NSW
- QLD
- SA
Work Type
- Full-time
Experience Level
- Minimum of 2 years of experience as a Clinical Research Associate
Education Level
- Bachelor's degree in a scientific or healthcare-related field
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
- At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
- As 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.