At a Glance
- Tasks: Manage and monitor clinical study sites to ensure successful trials.
- Company: Fortrea, a leader in innovative clinical research.
- Benefits: Career development, flexible work environment, and global impact.
- Other info: Extensive travel required; must have rights to work in Australia.
- Why this job: Join a team transforming healthcare through groundbreaking research.
- Qualifications: Bachelor’s degree in life sciences and 3 years of monitoring experience.
The predicted salary is between 82800 - 101200 $ per year.
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.
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Senior Clinical Research Associate I – Lead Site Monitoring employer: Fortrea
Fortrea is an exceptional employer for the Senior Clinical Research Associate II role, offering a dynamic work culture that prioritises employee growth and development. With a commitment to innovation in clinical research, employees benefit from comprehensive training programs, opportunities for advancement, and a supportive environment that values collaboration and integrity. Located in a vibrant area, Fortrea provides a unique advantage with access to cutting-edge resources and a network of professionals dedicated to making a meaningful impact in healthcare.
