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 Permanent (40 Hours per Week)
We are seeking a Research Assistant to support the Study Coordinator Team Lead and Study Coordinators in the coordination and delivery of early-phase clinical trials. This role supports protocol compliance, participant management and accurate study documentation to ensure high-quality research outcomes.
Key responsibilities include:
Supporting day-to-day coordination of clinical trial activities
Assisting with participant recruitment, screening and study visits
Ensuring compliance with study protocols, ICH/GCP and NZCR SOPs
Entering and maintaining accurate data in eCRFs and resolving EDC queries
Liaising with investigators, sponsors and laboratories
Maintaining accurate and up-to-date study documentation
Assisting with study initiation visits and related meetings
Skills and Experience
A tertiary qualification in a science-based discipline (or working towards one)
Strong attention to detail and scientific understanding
Knowledge of medical terminology
Excellent organisational and communication skills
Ability to work collaboratively in a team environment
Confidence using Microsoft Office and electronic systems
Experience in clinical research or knowledge of ICH/GCP is advantageous but not essential.
Additional Information
When you join us, we offer a range of benefits that work for you, your lifestyle and your career development which include:
Boost Employee Benefits Programme: currently offering seventy-seven benefits, such as health insurance, gym memberships, discounts for Torpedo7 and more.
Engage in a vibrant workplace within a rapidly expanding company, providing opportunities for continuous learning, personal growth, and success.
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.
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 Permanent (40 Hours per Week)
We are seeking a Research Assistant to support the Study Coordinator Team Lead and Study Coordinators in the coordination and delivery of early-phase clinical trials. This role supports protocol compliance, participant management and accurate study documentation to ensure high-quality research outcomes.
Key responsibilities include:
Supporting day-to-day coordination of clinical trial activities
Assisting with participant recruitment, screening and study visits
Ensuring compliance with study protocols, ICH/GCP and NZCR SOPs
Entering and maintaining accurate data in eCRFs and resolving EDC queries
Liaising with investigators, sponsors and laboratories
Maintaining accurate and up-to-date study documentation
Assisting with study initiation visits and related meetings
Skills and Experience
A tertiary qualification in a science-based discipline (or working towards one)
Strong attention to detail and scientific understanding
Knowledge of medical terminology
Excellent organisational and communication skills
Ability to work collaboratively in a team environment
Confidence using Microsoft Office and electronic systems
Experience in clinical research or knowledge of ICH/GCP is advantageous but not essential.
Additional Information
When you join us, we offer a range of benefits that work for you, your lifestyle and your career development which include:
Boost Employee Benefits Programme: currently offering seventy-seven benefits, such as health insurance, gym memberships, discounts for Torpedo7 and more.
Engage in a vibrant workplace within a rapidly expanding company, providing opportunities for continuous learning, personal growth, and success.
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.
