Ground every answer in facts on this page and the original listing. We never invent Glassdoor-style reviews or salaries that are not in our data.
Strong fit if you enjoy meticulous data prep and analysis in a clinical research context, prefer structured on-site work in Penrose/Auckland, and can turn messy inputs into defensible, report-ready outputs. Thin public company intel means culture and level should be confirmed in the process.
As a Data Specialist at New Zealand Clinical Research in Penrose, a typical day centres on preparing and checking research datasets: organising raw inputs, flagging inaccuracies, and weighting or adjusting data before analysis. You may assess whether statistical methods fit the study questions, run analyses that highlight meaningful patterns, and package findings as tables, charts, or short reports for study teams. Accuracy and audit-ready documentation matter as much as speed.
No — the listing is on-site in Penrose, Auckland City.
Tasks aligned with statistical data work: prepare and validate data, choose suitable methods, analyse, and report results clearly.
O*NET’s summary for SOC 15-2041.00 at onetonline.org lists related tasks and skills.
Public-domain labor data — prepare examples for 2–3 of these.
Data Specialist - New Zealand Clinical Research - Penrose, Auckland City What This Role Involves The Data Specialist will play a critical role in ensuring the accuracy and integrity of data collected from clinical trials. Responsibilities include managing databases, conducting data validation, preparing reports, and collaborating with cross-functional teams to ensure compliance with regulatory standards. What You'll Do Manage and maintain clinical trial databases using industry-standard software tools. Conduct thorough data validation and cleaning to ensure accuracy and completeness of data. Create and distribute regular reports on data trends, findings, and issues to stakeholders. Collaborate with project teams to identify and resolve data-related challenges during clinical trials. Ensure adherence to regulatory requirements and best practices in data management. Requirements A degree in Biostatistics, Data Science, or a related field is required. At least 3 years of experience in clinical research with a focus on data management. Familiarity with statistical software and database management systems (e.g., SAS, SQL). Strong attention to detail and ability to work accurately under pressure. Excellent communication skills for working across multiple departments. About New Zealand Clinical Research New Zealand Clinical Research was established in 2020 through the merger of Auckland Clinical Studies (ACS) and Christchurch Clinical Studies Trust (CCST). With over 35 years of combined research excellence, NZCR has successfully completed 750 trials involving 15,000 participants. Our mission is to advance medical knowledge and improve patient outcomes by leading in early-phase clinical research. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
Generated for personal interview prep · 2026-07-25 UTC · getajob.ai