🏠 Lead Oncology Clinical Trials as Senior CRA - Melbourne (Home-Based)
Join ICON plc in Melbourne as a Senior Clinical Research Associate and embrace an exciting FSP opportunity with a growing biotech company. This home-based role offers the unique chance to manage the complete site lifecycle of cutting-edge oncology trials while working from anywhere in Melbourne, with travel to leading clinical sites across Australia.
🎯 Your Impact: Key Responsibilities
End-to-End Site Management
- Manage the complete clinical trial lifecycle from site selection through initiation, monitoring, and close-out
- Conduct comprehensive site visits to assess performance, resolve complex issues, and ensure successful oncology trial execution
- Provide expert training and guidance to site staff, fostering high standards in oncology clinical research
- Build and maintain effective relationships with oncology investigators and site personnel across Australia
Oncology Trial Excellence
- Monitor clinical trial sites to ensure strict adherence to oncology-specific protocols and GCP standards
- Collaborate with cross-functional teams to ensure accurate data collection and reporting for oncology studies
- Leverage oncology expertise to support sites in managing complex patient populations and treatment regimens
- Serve as oncology subject matter expert for assigned sites throughout the trial lifecycle
Quality & Compliance Leadership
- Ensure data integrity and participant safety through meticulous monitoring practices
- Drive compliance within Australia's regulatory environment for oncology clinical trials
- Utilize clinical trial software and tools to optimize monitoring efficiency and data quality
- Maintain audit-ready documentation and processes for regulatory inspections
Biotech Partnership
- Work exclusively with an innovative small biotech company through ICON's FSP program
- Contribute to groundbreaking oncology research in a dynamic, growth-oriented environment
- Take ownership of site management with greater autonomy and responsibility
- Help shape clinical development strategies for emerging oncology therapies
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Advanced degree in life sciences, nursing, medicine, or related field
- Extensive experience as a Clinical Research Associate with strong understanding of clinical trial processes
- Proven ability to manage multiple sites and projects simultaneously
- Experience with site start-up activities and full trial lifecycle management
Oncology Expertise
- Background in oncology clinical trials preferred
- Understanding of oncology-specific endpoints and response criteria
- Experience with complex oncology protocols and patient management
- Knowledge of oncology imaging requirements and adverse event monitoring
Professional Competencies
- Strong organizational and problem-solving skills for complex study challenges
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to influence and drive compliance in complex regulatory environments
- Proficiency in clinical trial software and monitoring tools
Operational Requirements
- Ability to travel approximately 60% domestically across Australia
- Valid driver's license for site visit requirements
- Home-based in Melbourne with reliable internet and dedicated workspace
- Flexibility to accommodate varying site schedules and study demands
💫 Why Join This FSP Opportunity?
Biotech Innovation
- Exclusive partnership with a growing small biotech company
- Opportunity to contribute to cutting-edge oncology research from early development
- Greater autonomy and ownership of site management activities
- Direct impact on the success of innovative cancer therapies
Home-Based Flexibility
- Work from anywhere in Melbourne with flexible remote arrangement
- Balance extensive site travel with comfortable home office environment
- Avoid daily commute while maintaining professional collaboration
- Modern technology infrastructure for seamless virtual teamwork
Career Advancement
- Clear pathway to Clinical Team Lead and Project Management roles
- Exposure to novel oncology therapies and development strategies
- Opportunities for professional development in specialized monitoring techniques
- Growth potential within both ICON and the partner biotech organization
Melbourne Advantages
- Access to leading clinical research sites and oncology centers
- Vibrant healthcare and life sciences community
- Professional networking opportunities in Australia's medical research hub
- Supportive local team with national and global collaboration
Competitive Australia Benefits
- Attractive salary package with performance incentives and travel allowances
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave with Australian public holidays
Additional Benefits
- Retirement planning through superannuation benefits
- Life assurance coverage
- Professional development allowance and training opportunities
- Health and wellness programs
- Travel and accommodation support for site monitoring
✨ Ready to Drive Oncology Innovation from Melbourne?
If you're an experienced CRA with passion for oncology research and interest in biotech partnership, we encourage you to apply. This home-based Senior CRA role offers the unique opportunity to manage complete site lifecycles while contributing to groundbreaking cancer research from your Melbourne home base.
Apply Now & Lead Oncology Trial Excellence in Australia!
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ICON is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We welcome applications from all qualified clinical research professionals across Melbourne and Australia - your oncology expertise and site management experience might be exactly what we need for this exciting biotech partnership!
