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.
Skills Required
- Bachelor's degree in life sciences or related field
- Minimum of 3 years clinical onsite monitoring experience
- Strong knowledge of regulatory requirements
- Proficiency in relevant computer applications and systems
- Valid driver's license and ability to travel
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
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