Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Adelaide or Brisbane
Description
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 I, 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:
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Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.
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Ensure patient safety and compliance with informed consent and protocol requirements.
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Review source documents and verify data integrity on Case Report Forms (CRFs).
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Prepare accurate and timely monitoring reports and maintain study files.
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Serve as lead monitor for assigned protocols and assist in developing monitoring plans.
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Coordinate with vendors and internal teams to meet project timelines and objectives.
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Support feasibility assessments, budget negotiations, and regulatory submissions.
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Mentor and train junior team members through co-monitoring and guidance.
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Travel extensively (60–80%) to support site activities and maintain audit readiness.
Qualifications
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Bachelor’s degree in life sciences or related field, or equivalent clinical research experience.
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Typically a minimum of 3 years clinical onsite monitoring experience in pharmaceutical or CRO settings.
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Strong knowledge of regulatory requirements and drug development processes.
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Advanced site management skills.
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Excellent communication, organizational, and problem-solving abilities.
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Proficiency in relevant computer applications and systems.
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Valid driver’s license and ability to travel extensively.
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Have the rights to work in Australia. Sorry, no visa sponsorship support offered at this time.
Why Join Fortrea?
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Global Impact: Contribute to groundbreaking research that improves lives worldwide.
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Career Development: Access robust training, mentorship, and advancement opportunities.
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Flexibility & Support: Thrive in a collaborative, inclusive environment that values work-life balance.
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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.
Fortrea is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Learn more about our EEO & Accommodations request here .