Clinical Research Associate 1 at IQVIA. - Turkey

Melbourne, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

31 Dec, 25

Salary

0.0

Posted On

02 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Site Visits, Recruitment Strategies, Training, Communication, Quality Assurance, Regulatory Compliance, Data Management, Documentation, Team Collaboration, Financial Management, GCP Knowledge, ICH Knowledge, Tech Savvy, Proactive Mindset, Strong Communication Skills, Passion for Excellence

Industry

Hospitals and Health Care

Description

Are you passionate about science, driven by purpose, and ready to make a real impact in the world of clinical research? We’re looking for a Clinical Research Associate 1 who’s ready to take their career to the next level—working on cutting-edge studies that shape the future of medicine. Ideally Sydney or Melbourne. This role is on our Single Sponsor team Please note as part of the assessment you will be asked to complete a short video screening interview. 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. What You Bring A degree in life sciences or healthcare (or equivalent experience). 12 months minimum on-site Independant monitoring experience to be considered, ideally haemotology. Deep knowledge of GCP, ICH, and clinical trial operations. Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad). A proactive mindset, strong communication skills, and a passion for excellence. Why Join Us? Work on diverse, global studies across multiple therapeutic areas. Be part of a supportive, innovative team that values your growth. Enjoy flexible work arrangements, travel opportunities, and career develop 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 IQVIA 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.

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Responsibilities

The Clinical Research Associate 1 will engage in site visits, develop recruitment strategies, and provide training to ensure study success. They will monitor study progress, maintain documentation, and manage site financials.