At a Glance
- Tasks: Coordinate regulatory submissions and liaise with investigative sites to ensure project timelines.
- Company: Fortrea, a leader in clinical trials with a focus on innovation.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Fast-paced environment with a focus on quality and audit readiness.
- Why this job: Join a dynamic team and play a crucial role in advancing medical research.
- Qualifications: Knowledge of ICH/GCP and strong organisational skills required.
The predicted salary is between 81000 - 99000 $ per year.
Fortrea is seeking a regulatory submissions specialist to act as the primary liaison with investigative sites.
You will collect and compile essential documents, ensure timely IRB/IEC and authority submissions, and coordinate with internal teams and vendors to maintain project timelines.
The role requires knowledge of ICH/GCP, regulatory guidelines, and a proactive approach to risk escalation, with a focus on audit readiness and quality review.
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Clinical Trials Start-Up Specialist in Sydney 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.
