Senior Clinical Research Associate I - Sydney Melbourne Adelaide or Brisbane

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:** * 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 of 3 years clinical onsite monitoring experience in pharmaceutical or CRO settings. * Strong knowledge of regulatory requirements and drug development processes. * Advanced site 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. * Have the rights to work in Australia. _Sorry, no visa sponsorship support offered at this time._ **Why Join Fortrea?** * **Global Impact:** Contribute to groundbreaking research that improves lives worldwide. * **Career Development:** 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. 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](https://careers.fortrea.com/us/en/eeo-and-accommodations).