(Senior) Clinical Research Associate
Apply locations: North Sydney, New South Wales, Australia; Melbourne, Australia
Time type: Full time
Posted on: Posted Yesterday
Time left to apply: End Date: January 31, 2025 (30+ days left to apply)
Job requisition id: R1457413
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. Currently seeking a Senior Clinical Research Associate in Sydney or Melbourne. This will be in our FSP team. You must have a minimum of 4 years independent on-site monitoring experience to be considered for this role. We regret to inform that we cannot consider sponsorship for this role, 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.
Essential Functions: Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes.Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.Qualifications: Educational Excellence: Bachelor's degree in a scientific or healthcare discipline preferred.Experience Matters: At least 4 years of on-site monitoring experience (across Australia), with preference for Oncology trial management exposure.Regulatory Savvy: Strong knowledge of GCP and ICH guidelines.Tech-Savvy: Proficiency in Microsoft Office and relevant technology.Communication Pro: Excellent written and verbal skills.Organized and Analytical: Strong organizational and problem-solving abilities.Time and Financial Management: Effective in managing time and finances.Team Player: Ability to build and maintain strong relationships with coworkers, managers, and clients.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 at https://jobs.iqvia.com
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