š„ Launch Your Clinical Research Career in Sydney
JoinĀ ICON plcĀ as aĀ Clinical Site AssociateĀ in our modern Sydney offices and build the foundation for an exciting career in clinical research. This office-based role offers comprehensive exposure to clinical trial operations while working alongside industry experts in Australia's vibrant healthcare sector.
šÆ Your Impact: Key Responsibilities
Clinical Trial Support & Coordination
- Assist in planning, initiating, and executing clinical trial activities
- ConductĀ site feasibility assessmentsĀ and participate in site selection processes
- Coordinate with investigative sites to ensureĀ protocol complianceĀ and regulatory adherence
- Monitor study progress and data collection activities for quality and accuracy
Documentation & Compliance Management
- Assist in preparation and review of study documentation and reports
- Support regulatory compliance and essential document management
- Help maintainĀ Trial Master Files (TMF)Ā to inspection-ready standards
- Ensure adherence toĀ ICH-GCP guidelinesĀ and Australian regulatory requirements
Site Management & Communication
- Serve as primary in-house contact for clinical sites across Australia
- Facilitate effective communication between sites and study teams
- Support site training and investigator relationship management
- Track site performance metrics and enrollment progress
Operational Excellence
- Maintain accurate study timelines and tracking systems
- Participate in cross-functional team meetings and training
- Support quality control and process improvement initiatives
- Assist with data management and query resolution processes
ā Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree inĀ Life Sciences, Healthcare, or related field
- Understanding of clinical research principles andĀ ICH-GCP guidelines
- Strong organizational skills with excellent attention to detail
- Effective communication and collaboration abilities
Preferred Experience
- Previous exposure to clinical research or healthcare environment
- Experience with clinical trial documentation and processes
- Knowledge of Australian regulatory landscape
- Proficiency with clinical trial management systems
Professional Attributes
- Ability to prioritize tasks and manage multiple responsibilities
- Proactive problem-solving mindset
- Strong interpersonal and relationship-building skills
- Adaptability in fast-paced environment
- Commitment to quality and continuous improvement
š« Why Join ICON in Sydney?
Career Development Pathway
- Comprehensive CSA training and development program
- Clear progression path toĀ Clinical Research Associate (CRA)Ā role
- Mentorship from experienced clinical research professionals
- Exposure to global clinical trials across multiple therapeutic areas
Professional Workplace
- Modern office facilities in strategic Sydney location
- Collaborative team environment with global connectivity
- Structured onboarding and ongoing training support
- Access to cutting-edge clinical research technology
Competitive Benefits Package
- Attractive entry-level salary with performance incentives
- Comprehensive health insurance coverage
- Retirement planning and financial wellness programs
- Generous vacation entitlements and flexible work options
- Global employee assistance and wellbeing support
āØ Begin Your Clinical Research Journey Today
If you're passionate about starting a career in clinical research and possess the foundational skills we're looking for, we encourage you to apply. At ICON, we value potential and dedication - your attitude and eagerness to learn are just as important as your existing experience.
Apply Now & Build Your Future in Healthcare Innovation
