About this role
Established in 2020 through the merger of Auckland Clinical Studies (ACS) and Christchurch Clinical Studies Trust (CCST), NZCR is at the forefront of early-phase clinical research in New Zealand. With over 35 years of combined research excellence, we have successfully completed 750 trials involving 15,000 participants, showcasing our commitment to advancing medical research. Our physician-led, world-class research units in Auckland, Christchurch, Wellington, and Hamilton conduct complex studies in both healthy participants and patient populations. Partnering with global pharmaceutical and biotech companies, we deliver excellence in clinical research and explore potential new medicines. Recognizing the pivotal role of study participants, NZCR prioritizes their safety and comfort through detailed study information, expert clinical care, and comprehensive support services.
The Role
Full Time, Fixed Term - 12 September 2026 until 12 September 2027
The purpose of this role is to support the planning, coordination, and administration of late phase clinical trials under the supervision of the Study Coordinator Team Lead. The role contributes to the management of the study life cycle, including patient-facing activities, study documentation, and data integrity, while ensuring compliance with NZCR Policies and Procedures, study protocols, Good Clinical Practice Guidelines (ICH-GCP), and applicable regulatory requirements.
Skills and Experience • Minimum bachelor's degree (Science or related field) • At least 1 year of experience related to the key tasks for this role • Experience with real-time eSource platforms and clinical trial systems is an advantage • Familiarity with Interactive Response Technology (IRT) systems is an advantage
For more information about NZCR visit www.nzcr.co.nz.
If you are interested in this great opportunity and you are available, please click Apply for this job to submit your CV and cover letter.
To apply for this role, you MUST be a NZ resident with a valid work visa.
When you apply for this role, you are consenting to us sharing your information with our sister company, Optimal, where additional opportunities for career growth and development may arise.