Associate Study Coordinator

NZCR; Christchurch; On-site; NZD 60,000 - 80,000; Full time

Benefits offered by this job

Boost Employee Benefits Programme

Gym memberships

Discounts (Torpedo7)

Job summary

NZCR is seeking a dedicated Clinical Trials Coordinator to plan, coordinate and administer clinical trials under the supervision of the Senior Clinical Trial Leader. This full-time, fixed-term role spans 6–7 months and covers the project lifecycle with strict adherence to study protocols and regulatory guidelines.

The successful candidate will hold a Bachelor’s degree in Science and have at least one year of related experience. NZ residency with a valid work visa is required.

Qualifications

• Bachelor’s degree in Science or equivalent.
• At least 1 year of experience related to the key tasks for this role.

Responsibilities

• Plan, coordinate and administer clinical trials under supervision of the Senior Clinical Trial Leader.
• Manage the project life cycle to ensure delivery of objectives and compliance with NZCR policies, protocols, GCP and regulatory requirements.

Skills

Experience in clinical trials

Education

Bachelor’s degree (Science)

Job description

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 6-7 months

The purpose of this role is to plan, coordinate, and administer clinical trials under the supervision of the Senior Clinical Trial Leader (SCTL). The role is responsible for managing the project life cycle to ensure effective delivery of objectives 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)
• At least 1 year of experience that is related to the key tasks for this role.

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 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.

To apply for this role, you MUST be a NZ resident with a valid work visa.