Clinical Research Jobs at Fortrea, Melbourne
Fortrea is seeking a Senior Clinical Research Associate I (SCRA I) to support clinical trials under the FSP (Functional Service Provider) model. This full-time, hybrid role involves leading site monitoring and site management activities while ensuring compliance with regulatory guidelines and standard operating procedures. The Clinical Research Jobs at Fortrea Careers offer opportunities to contribute to high-quality clinical research while working independently and collaboratively on projects of limited scope.
Job Details:
- Position Title: Senior Clinical Research Associate I (SCRA I)
- Job Requisition ID: 254363
- Employment Type: Full-Time
- Work Model: Hybrid
- Location: Melbourne, Australia
- Travel Requirement: 60–80%
- Industry: Clinical Research / CRO
About the Company:
Fortrea is a leading global contract research organization (CRO) delivering clinical development solutions across the drug and device development lifecycle. With a strong focus on scientific rigor, regulatory compliance, and patient safety, Fortrea partners with sponsors worldwide to accelerate the delivery of life-changing therapies.
Educational Requirements for the Clinical Research Associate Role:
- University or college degree (Life Sciences preferred)
- OR certification in a related allied health profession
- OR minimum of 3 years of relevant clinical research experience in pharmaceutical or CRO industries (in lieu of formal education)
Key Responsibilities of the Clinical Research Associate:
- Perform all aspects of clinical site monitoring, including routine visits and site closeouts
- Conduct pre-study, site initiation, monitoring, and close-out visits
- Maintain accurate and complete study documentation and site files
- Manage study sites in accordance with project plans and regulatory guidelines
- Ensure compliance with Fortrea and sponsor SOPs and regulatory requirements
- Liaise with vendors and cross-functional teams as required
- Support project plan implementation and assigned project leadership roles
- Act as Lead CRA, Local Project Coordinator, or line manager when assigned
- Oversee Serious Adverse Event (SAE) reporting, follow-up, and documentation
Skills Required for the Clinical Research Associate Role:
- Strong knowledge of global regulatory requirements
- Thorough understanding of the drug development process
- Advanced clinical site monitoring and site management skills
- Experience with SAE reporting, narratives, and follow-up
- Advanced registry administration skills
- Ability to work independently with minimal supervision
- Strong written and verbal communication skills in English and local language
- Excellent organizational and leadership capabilities
- Valid driver’s license and willingness to travel extensively
Benefits of the Clinical Research Jobs at Fortrea Careers:
- Opportunity to work in a global CRO environment
- Exposure to diverse clinical trials under the FSP model
- Leadership and project coordination responsibilities
- Professional growth in clinical research and regulatory compliance
- Hybrid working model offering flexibility
- Competitive compensation and career development opportunities
