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Global Clinical Trials Specialist
3 weeks ago
As a leading global contract research organization, we provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in over 100 countries, we are transforming drug and device development for partners and patients worldwide.
Main Responsibilities:
- Monitoring cutting-edge global clinical trials, ensuring data integrity and compliance with regulatory requirements
- Liaising with vendors, managing study sites, and conducting pre-study and initiation visits
- Maintaining accurate records, verifying informed consent procedures, and ensuring protocol adherence
- Ensuring the protection of study patients, monitoring serious adverse events, and reporting accordingly
Requirements:
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution
- Demonstrated experience of at least 18 months in onsite monitoring global clinical trials from SIV to Close-out
- Understanding of local regulatory guidelines, ability to travel interstate for site visits
- Happy to split time working from an office and home (Hybrid)
Benefits:
- Opportunities to work on diverse global clinical trials, develop skills, and advance career
- Supportive managers, career development pathways, and opportunities for growth
- Access to AI-assisted technology to ease workload and enhance productivity
About Us:
We are a leading global contract research organization, committed to delivering high-quality clinical development solutions. Our team is passionate about scientific rigor, and we pride ourselves on our expertise in clinical development, patient access, and technology solutions.
Join Our Team:
If you are a motivated professional with a passion for clinical research, we encourage you to apply for this exciting opportunity.