Senior Clinical Research Associate I/II - FSP - Sydney or Melbourne
- LocationSydney; Melbourne
- Work typeHybrid
- EmploymentFull-time
- Posted11 November 2026
- SourceFortrea's careers page (Workday)
Live checkFirst seen 7 h ago; still listed on Fortrea's careers page 1 h ago.
At a glance
- Experience3+ years
- EducationBachelor's degree or equivalent
- Skills and toolsDriver's license
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About the role
Shape the Future of Clinical Research with Fortrea
At Fortrea, we are redefining the clinical research landscape through innovation, collaboration, and a commitment to improving health worldwide. Join a global team where your expertise drives meaningful impact, and your career growth is supported every step of the way.
About the Role
As a Senior Clinical Research Associate, you will play a pivotal role in ensuring the success of clinical trials by managing and monitoring study sites. You’ll work closely with investigators and sponsors to uphold regulatory standards and deliver high-quality data that advances medical breakthroughs.
Key Responsibilities :
- Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.
- Ensure patient safety and compliance with informed consent and protocol requirements.
- Review source documents and verify data integrity on Case Report Forms (CRFs).
- Prepare accurate and timely monitoring reports and maintain study files.
- Serve as lead monitor for assigned protocols and assist in developing monitoring plans.
- Coordinate with vendors and internal teams to meet project timelines and objectives.
- Support feasibility assessments, budget negotiations, and regulatory submissions.
- Mentor and train junior team members through co-monitoring and guidance.
- Travel extensively (60–80%) to support site activities and maintain audit readiness.
Qualifications
- Bachelor’s degree in life sciences or related field, or equivalent clinical research experience.
- Typically a minimum 3 years of clinical monitoring experience in pharmaceutical or CRO settings.
- Strong knowledge of regulatory requirements and drug development processes.
- Advanced site monitoring and management skills.
- Excellent communication, organizational, and problem-solving abilities.
- Proficiency in relevant computer applications and systems.
- Valid driver’s license and ability to travel extensively.
Why Join Fortrea ?
- Global Impact: Contribute to groundbreaking research that improves lives worldwide.
- Career Growth: Access robust training, mentorship, and advancement opportunities.
- Flexibility & Support: Thrive in a collaborative, inclusive environment that values work-life balance.
- Innovation: Be part of a forward-thinking organization shaping the future of clinical trials.
Ready to make a difference? Apply today and be part of a team that’s transforming healthcare.
Learn more about our EEO & Accommodations request here .
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