Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Perth, Ad at Fortrea

Sydney, New South Wales, Australia -

Full Time

Start Date

Immediate

Expiry Date

30 Jul, 26

Salary

0.0

Posted On

01 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical monitoring, Site management, Regulatory compliance, Data integrity, Protocol management, Source document verification, Feasibility assessment, Budget negotiation, Mentoring, Communication, Problem-solving, Organizational skills

Industry

Biotechnology Research

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: 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. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. 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.

Responsibilities

The Senior Clinical Research Associate manages and monitors clinical study sites to ensure patient safety and protocol compliance. They are responsible for verifying data integrity, preparing monitoring reports, and mentoring junior team members.