Clinical Data Coordinator

NZCR Clinical Trials; Christchurch; On-site; NZD 60,000 - 75,000; Full time

Benefits offered by this job

Gym memberships

Discounts for Torpedo7

Career development opportunities

Job summary

NZCR Clinical Trials in Christchurch is seeking a Clinical Data Coordinator to ensure the accuracy and integrity of clinical trial data. You will transcribe source data into sponsor EDC systems and resolve data queries across studies.

Responsibilities include maintaining data entry timelines, supporting quality control, and liaising with study coordinators, clinical teams and CRAs. NZ residency with a valid work visa is required.

Qualifications

• Tertiary qualification in a science-based discipline (or working towards one).
• Excellent attention to detail and accuracy.
• Knowledge of science and medical terminology.
• Strong communication and teamwork skills.
• Proficiency in Microsoft Office and computer systems.
• Ability to manage deadlines and prioritise workload.

Responsibilities

• Identifying and resolving data discrepancies and queries
• Maintaining data entry and query resolution timelines
• Supporting quality control activities and discrepancy reviews
• Liaising with Study Coordinators, clinical teams, and CRAs
• Ensuring compliance with Good Clinical Practice (GCP) and study protocols

Skills

Attention to detail

Data entry

Communication skills

Teamwork

Microsoft Office

Medical terminology

Education

Science degree (or pursuing)

Tools

EDC systems

Job description

The Role

Full-Time, Permanent

As a Clinical Data Coordinator, you will ensure the accuracy and integrity of clinical trial data. You will transcribe source data into sponsor electronic data capture (EDC) systems, identify and resolve data queries, and support quality control processes across studies.

Key responsibilities

• Identifying and resolving data discrepancies and queries
• Maintaining data entry and query resolution timelines
• Supporting quality control activities and discrepancy reviews
• Liaising with Study Coordinators, clinical teams, and Clinical Research Associates (CRAs)
• Ensuring compliance with Good Clinical Practice (GCP) and study protocols

You MUST be a NZ resident with a valid work visa.

Skills and Experience

• Tertiary qualification in a science-based discipline (or working towards one)
• Excellent attention to detail and accuracy
• Knowledge of science and medical terminology
• Strong communication and teamwork skills
• Proficiency in Microsoft Office and computer systems
• Ability to manage deadlines and prioritise workload

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.