Clinical Research Associate - QLD

Overview

The Clinical Research Associate (CRAII - CRAIII) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from source documents. The CRA is the primary contact between the Investigational Sites, Novotech and the Sponsor, managing site relationships and ensuring clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech / Client SOPs.

Hybrid working arrangements and full flexibility in working hours are provided to support work‑life balance.

Minimum Qualifications & Experience

• Graduate in a clinical or life sciences‑related field.
• Relevant experience / qualifications in allied professions may be considered.
• Good time management skills, attention to detail, teamwork, and computer literacy.
• Experience in the research, pharmaceutical industry or a related field per level :

CRA II : minimum 6 months independent monitoring experience.

Responsibilities

Benefits

Novotech offers a supportive workplace with flexible working options, paid parental leave for both parents, flex leave entitlements, wellness programs, ongoing development opportunities and a commitment to an inclusive environment for all employees.

About Us

Novotech is a global full‑service clinical Contract Research Organization headquartered in Sydney, Australia with 34 offices across Asia‑Pacific, North America and Europe. With over 3,000 employees and 5,000 site partnerships, Novotech provides clinical development services across all phases of clinical trials, achieving the highest IT security and quality standards.

About the Team

Our team culture fosters partnership and collaboration, includes strategic and transactional mindsets, proactive decision making, senior stakeholder support, and a collaborative environment for career development across a diverse global organization.

Job Info

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