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This role suits candidates who like structured trial oversight, detail-heavy documentation, and stakeholder communication without heavy travel. Novotech’s New Zealand in-house CRA seat rewards organisation, GCP discipline, and calm problem-solving across active studies.
As an Inhouse Clinical Research Associate at Novotech in New Zealand, your day is desk-based trial oversight rather than constant site travel. Typical work includes reviewing monitoring reports and data queries, tracking enrolment and protocol deviations, coordinating with sites and project managers, and keeping eTMF and sponsor updates audit-ready.
Prioritise ICH-GCP, protocol and source-data review, query management, eTMF hygiene, and clear written updates to sites and sponsors. Build comfort with CTMS/EDC tools and risk-based monitoring concepts used in in-house CRA work.
The title signals an in-house CRA model, so most work is centralised monitoring and coordination rather than frequent on-site visits.
Clinical research operations exposure, ICH-GCP familiarity, and comfort with EDC/CTMS and query workflows are strong foundations.
The listing is in New Zealand (Aotearoa) and is not marked remote, so expect a local or office-linked arrangement.
Inhouse Clinical Research Associate - NZ — Novotech, New Zealand The Opportunity Novotech is seeking a dedicated Inhouse Clinical Research Associate (IHCRA) to support our clinical team in accordance with project requirements, ICH GCP guidelines, local or global regulatory requirements, and Novotech or Client SOPs. This role will be based 2 days from our Auckland office. Key Responsibilities Support the clinical team’s in-house activities on assigned projects. Coordinate and maintain project documentation and records. Ensure compliance with ICH GCP guidelines, local or global regulatory requirements, and Novotech or Client SOPs. Contribute to the overall success of the clinical research initiatives by providing accurate and timely support. Skills & Qualifications Demonstrated experience in clinical research or a related field. Familiarity with ICH GCP guidelines, local or global regulatory requirements, and Novotech or Client SOPs. Strong organizational skills and attention to detail. Excellent communication and interpersonal skills. Working at Novotech At Novotech, we value our employees' contributions and provide a supportive work environment that encourages professional growth. Our team is dedicated to delivering high-quality clinical research solutions for clients worldwide. If you are passionate about contributing to innovative medical advancements, this role may be the perfect fit for you. Ready 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.
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