Clinical Research Associate II

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, 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.

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.