About the client:

This leading CRO offers clinical solutions across Australia in the areas of research, trials, project management, data management, safety, and medical writing. With growing clientele, they are looking to expand their team in Australia, continuing to deliver accurate, cost-effective and quality clinical support.

What the role will entail:

• Oversee multiple clinical projects to ensure trials are running efficiently and accurately
• Manage Phase 1 clinical trials
• Conduct qualification, initiation, site management and closeout visits across your sites
• Evaluate the quality and integrity of the reported data, site efficacy, and drug accountability
• Ensure sites are compliant with SOP, ICH-GCP, FDA, and EMEA
• Initiate and maintain relationships with site staff
• Data evaluation, report writing, budget management, and feasibility assessments
• Contribute to patient strategies to meet enrolment timelines and study delivery

Requirements to apply:

• 12 months Australian monitoring experience
• Tertiary Science degree
• Excellent knowledge of GCP/ICH, FDA, EMEA and local regulations
• Organised, friendly and enthusiastic professional with effective communication skills 

Benefits:

• Home-based roles in Sydney Brisbane and Melbourne
• Home Office equipment and support provided
• Strong pipeline range of therapy areas
• Focussed on Phase I trials
• Permanent Full-Time positions
• Career development
• Local Monitoring Sites
• Opportunities for less travel
• Competitive salary packages
• A flexible, experienced and growing team

If you would like to discuss the role further, please feel free to send your CV via this link and a Next Day Consultant will be in contact or for other opportunities check out www.nextdayrecruitment.com.au 

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