Clinical Research Associate II

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 New Zealand as a CRA II, 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.

We regret to inform you that we cannot 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.

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, with preference for oncology trials and haematology.
• 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.