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

Fortrea; Australia; Hybrid; AUD 80,000 - 100,000; Full time

Benefits offered by this job

Career Development

Flexibility & Support

Global Impact

Job summary

Fortrea is seeking a Senior Clinical Research Associate I in Australia to manage and monitor clinical study sites. The role involves ensuring compliance with regulatory standards and delivering high-quality data to advance medical breakthroughs. Candidates should have a Bachelor’s degree in life sciences, at least 3 years of onsite monitoring experience, and strong knowledge of regulatory requirements. The position offers career development opportunities and values work-life balance.

Qualifications

• 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.

Responsibilities

• Monitor and manage clinical study sites, including initiation and routine visits.
• Ensure patient safety and compliance with informed consent requirements.
• Prepare accurate and timely monitoring reports.

Skills

Clinical monitoring

Regulatory knowledge

Communication skills

Organizational skills

Problem-solving

Education

Bachelor’s degree in life sciences or related field

Job description

Fortrea is a global team redefining clinical research, inviting professionals to contribute to impactful work.

About the Role

As a Senior Clinical Research Associate I, you will manage and monitor clinical study sites, working 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.

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.