Job 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