Clinical Research Associate II

JobSpace; Auckland; Hybrid; NZD 90,000 - 120,000; Full time

Job summary

IQVIA in New Zealand is seeking a Clinical Research Associate (CRA) to monitor study sites and ensure high-quality, compliant conduct across trials. You will travel for site visits, support site activation, and collaborate with cross-functional teams in a hybrid work model.

Ideal candidates bring 4+ years of on-site monitoring, with oncology/haematology experience, strong GCP/ICH knowledge, and excellent communication and organizational skills to help drive study progress and patient outcomes.

Qualifications

• Bachelor's degree in a scientific or healthcare discipline preferred.
• At least 4 years of on-site monitoring experience, oncology trials and haematology preferred.
• Strong knowledge of GCP and ICH guidelines.
• Proficiency in Microsoft Office and relevant technology.
• Excellent written and verbal communication.
• Organized and analytical with strong problem-solving abilities.
• Time and financial management skills.
• Ability to build and maintain relationships with coworkers, managers and clients.

Responsibilities

• Engage in Site Visits: From selection to close-out, visits are pivotal for study success.
• Recruitment strategies: Develop and implement plans to recruit study subjects.
• Empower sites with knowledge: Provide training and maintain robust communication.
• Champion quality and integrity: Ensure adherence to protocols and regulations.
• Drive study progress: Monitor regulatory submissions and data query resolutions.
• Master documentation: Maintain meticulous site records.
• Collaborate and innovate: Work with a team to support project execution.
• Manage finances with precision: Oversee site financials and invoice retrieval.

Skills

GCP/ICH knowledge

Clinical monitoring

Communication

Organization

Time management

Education

Bachelor's degree in science/healthcare

Tools

Microsoft Office

Job description

Jora New Zealand will close on 9th September 2026. Thank you for being with us, we are cheering you on as you continue your career journey.

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, 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 can not 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.

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.

Where You'll Work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Senior Vice President Applied Data Science Center, R&D Solutions

Senior Director Global Site Activation

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what's possible for patients. Across every team and every corner of the globe, you'll find colleagues who genuinely care — about the mission and about each other. That's what makes this a place where people tend to stay, grow and do the best work of their careers.