Senior Clinical Research Associate 1

Senior Clinical Research Associate 1 page is loaded## Senior Clinical Research Associate 1locations: Melbourne, Australiatime type: Full timeposted on: Posted Todayjob requisition id: R Currently seeking Senior Clinical Research Associate for our Sponsor-dedicated team. Step into a dynamic role where you'll drive innovation and excellence in clinical research. As a key player in our team, you'll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare.When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.You must have a minimum of 5 years Independent on-site monitoring experience to be considered for this role with at least 3 years Oncology. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.You will be asked to complete a short video screening as part of the interview process.Melbourne is the preferred location at this stage Sydney can be considered### What You'll Do* Be the face of the study at site level—conducting selection, initiation, monitoring, and close-out visits with precision and purpose.* Drive subject recruitment strategies that deliver results and keep studies on track.* Deliver protocol training and build strong, collaborative relationships with site teams.* Champion quality and compliance, escalating issues and ensuring GCP/ICH standards are met.* Track study progress, manage documentation, and keep Trial Master Files audit-ready.* Mentor junior clinical staff and contribute to a culture of excellence and learning.* Collaborate with cross-functional teams to ensure seamless project execution.### ### What You Bring* A degree in a scientific or healthcare discipline (or equivalent experience).* 5+ years of Independant on-site monitoring experience. With a minimum 3 years oncology.* Deep knowledge of GCP, ICH, and clinical trial regulations.* Strong therapeutic area expertise and protocol understanding.* Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).* Excellent communication, organization, and problem-solving skills.* A proactive mindset and the ability to build strong relationships with stakeholders.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
#J-18808-Ljbffr