Clinical Research Associate II

IQVIA; Auckland; On-site; NZD 90,000 - 120,000; Full time

Job summary

IQVIA in New Zealand is seeking a CRA II to drive site engagement and study execution. You will oversee on-site monitoring from site selection through closeout, supporting recruitment strategies and training to ensure compliant, high‑quality data across multiple therapeutic areas.

We require a Bachelor’s degree in a scientific/healthcare field and at least 4 years of on-site monitoring experience, preferably in oncology/haematology, with strong GCP/ICH knowledge.

Qualifications

• Bachelor’s degree in a scientific or healthcare field preferred.
• At least 4 years of on-site monitoring experience, oncology/haematology preferred.
• Strong knowledge of GCP and ICH guidelines.
• Proficiency in Microsoft Office and related technology.
• Excellent written and verbal communication.
• Strong organizational and analytical skills.
• Ability to manage time and project finances.
• Ability to build strong relationships with team and clients.

Responsibilities

• Engage in site visits from site selection to study close‑out.
• Develop and implement innovative recruitment plans for subjects.
• Provide training and maintain robust communication with sites.
• Evaluate and ensure adherence to protocols and regulatory requirements.
• Monitor study progress from regulatory submissions to data queries.
• Keep meticulous site documentation and source records.
• Collaborate with a passionate team to support project execution.
• Oversee site financials and ensure timely invoice retrieval.

Skills

Communication

Organizational skills

Analytical thinking

Time management

Financial management

Team player

Education

Bachelor's degree in science/healthcare

Tools

Microsoft Office

Job description

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.

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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.