About the Role
This is a senior position that requires extensive experience in clinical research, with a focus on site visits, recruitment strategies, and quality assurance.
* Key responsibilities include engaging with study sites, developing innovative recruitment plans, empowering sites with knowledge, championing quality and integrity, driving study progress, and master documentation.
* The ideal candidate will have at least 4 years of on-site monitoring experience, preferably in oncology trial management, and strong knowledge of GCP and ICH guidelines.
Benefits
This role offers stability, resources, and direct experience with customers. You will enjoy world-class training and mentoring, as well as opportunities to work in various therapeutic areas.
* A minimum of 4 years of independent on-site monitoring experience is required.
* Preferably located in Sydney or Melbourne, this role involves working closely with a passionate team to support project execution and drive success.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We create intelligent connections to accelerate medical treatments and improve patient outcomes worldwide.
Clinical Research Associate roles are available in Perth, Western Australia, among other locations.