Research Coordinator

Overview

Research Coordinator (Project Management)

Private Clinical Trial Site - Auckland

An opportunity to join one of New Zealand's leading early-phase clinical research organisations.

This company have been established for over 20 years and so are specialised experts in the industry.

They have a focus on neurology, oncology and diabetes clinical trials and have some fascinating projects focusing on gene editing and so offer some unique and complex studies.

They have seen some successes over the years and are a growing business, offering chances for progression and development across the teams.

You can see yourself growing into a Research Manager and above.

They are looking for a Research Coordinator to join on a permanent basis where you will be responsible for project managing multiple studies in a range of therapeutic areas.

This role would suit an experienced Clinical Trial Coordinator looking for their next challenge.

Responsibilities

Coordinate and oversee all aspects of clinical research studies, ensuring compliance with protocols, regulations, and ethical guidelines.

Recruit, screen, and enroll eligible study participants, ensuring accurate documentation and informed consent.

Schedule and conduct study visits, procedures, and follow-up assessments according to study protocols.

Collect, manage, and analyse research data, maintaining accurate and complete records.

Liaise with study sponsors, principal investigators, and interdisciplinary teams to facilitate study implementation and resolve any issues that arise.

Assist in the preparation and submission of regulatory documents, including Institutional Review Board (IRB) applications and study amendments.

Monitor and maintain study supply inventory, ensuring availability of necessary materials and equipment.

Collaborate with study participants and provide education and support throughout the research process.

Qualifications

Bachelor's degree in a health-related field, such as biology, nursing, or life sciences.

A relevant master's degree is a plus.

Previous experience as a Clinical Research Coordinator or in a similar research role is preferred.

Strong understanding of clinical research processes, regulations, and ethical guidelines (e.g., ICH-GCP).

Excellent organisational skills with the ability to multitask and prioritise tasks effectively.

Proficiency in data collection, management, and analysis.

Joining the team as a Clinical Research Coordinator will provide an opportunity to grow and become established in the area of clinical research.

They have a real focus on wellness and offer extensive leadership programmes to drive a healthy workforce.

If you are interested in this opportunity, then please apply direct or contact Keeley Munday on

Locations

Gold Coast, Queensland, Australia (On-site)

Indianapolis, Indiana, United States (On-site)

Lebanon, Indiana, United States (On-site)

Location Indiana, United States (On-site)

Slough, England, United Kingdom (On-site)

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