- Experience
- 4+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 2 weeks ago
- Work mode
- In office
- Education
- Bachelor's degree in a scientific or healthcare discipline preferred
- Eligibility
- Applicants must have full legal work rights for New Zealand; sponsorship is not available for this role.
- Resume
- Required to apply
Where you'll work
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Job description
Overview
Join an innovative and progressive clinical research team focused on advancing healthcare through rigorous study site management. As a Clinical Research Associate II with IQVIA New Zealand, you will be integral in ensuring study sites meet compliance standards while thriving in their roles, contributing to pioneering healthcare developments.
Benefit from the resources of a renowned global contract research organization and gain diverse therapeutic area experience enhanced through world-class training and mentoring. Note that sponsorship is not available; applicants must hold full work rights. Candidates will undergo a brief video screening as part of the interview process.
Primary Responsibilities
- Conduct site visits throughout all phases, from site selection through to study close-out, to support successful study execution.
- Design and implement innovative participant recruitment strategies impacting clinical trial progress.
- Provide comprehensive training and maintain clear communication to empower study sites.
- Assess and improve site compliance with study protocols and regulatory requirements to uphold quality and integrity.
- Oversee progress monitoring including regulatory submission tracking and resolution of data queries.
- Ensure thorough documentation and accurate maintenance of site records.
- Collaborate closely with project teams to enhance execution and overall success.
- Manage site financials carefully, including timely processing of invoices.
Qualifications
- Bachelor’s degree in scientific or healthcare-related disciplines preferred.
- Minimum of four years’ on-site monitoring experience, with a preference for oncology and haematology trials.
- Strong familiarity with Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Proficient in Microsoft Office suite and related technologies.
- Exceptional written and oral communication skills.
- Highly organized with strong analytical and problem-solving capabilities.
- Effective time and financial management skills.
- Ability to foster positive relationships with colleagues, management, and clients.
Company Background
IQVIA is a renowned global leader delivering clinical research services, commercial insights, and healthcare intelligence to life sciences and healthcare sectors. The organization connects expertise to expedite development and commercialization of innovative therapies aimed at improving patient outcomes worldwide.
Important Notes
IQVIA enforces strict integrity standards throughout recruitment, with zero tolerance for any candidate deception. All information and credentials must be accurate and complete to avoid disqualification or employment termination in compliance with applicable laws.
Minimum education
Bachelor's Degree