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Senior Clinical Research Associate I/II - FSP - Sydney or Melbourne

Hiring from
Australia
Work type
Hybrid
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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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At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

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