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 Clinical Research Associate II role.
Rezi rewrites your resume against ICON plc's job description. Free.
Tailor your resume to this Clinical Research Associate 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 Clinical Research Associate II posting at ICON plc — free, in seconds.
Don't guess if your resume is good enough.
See how it scores against the Clinical Research Associate II posting at ICON plc — free, in seconds.
About the Role
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Responsibilities
- 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.
Requirements
- Minimum of 2 years of independent monitoring experience as a Clinical Research Associate within CRO/Pharma.
- 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.
- Ability to travel locally and interstate and should possess a valid driver’s license.
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Skills
- Organizational skills
- Communication skills
- Attention to detail
Location
- Australia
Work Type
- Home-based
- Remote
Experience Level
- 2 years of independent monitoring experience
Education Level
- Bachelor's degree in a scientific or healthcare-related field.
Salary/Compensations
- Competitive base salary
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 a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
- As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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.