Senior Clinical Research Associate I (SCRA1) - Sydney, Melbourne, Perth, Adelaide or Brisbane

Sydney, AustraliaOn-site

Responsibilities

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.
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.
Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.

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
Advanced site management skills.
Proficiency in relevant computer applications and systems.
Valid driver’s license and ability to travel extensively.

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