The Role
Full-Time, Permanent
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
This opportunity is well suited to our current Research Assistants or Associate Study Coordinators who are passionate about patient engagement, education, and contributing to high-quality research that improves health outcomes. We are interested in hearing from individuals who demonstrate strong organisational and communication skills, attention to detail, and the ability to work effectively within a multidisciplinary team.
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