Hybrid CRA II/III – Flexible Hours & Site Leadership

Novotech; Sydney; Híbrido; AUD 70.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work arrangements

Flexible working hours

Descripción de la vacante

Novotech is seeking a Clinical Research Associate (CRA) to safeguard trial participant welfare and ensure accurate, verifiable data across source documents. The CRA acts as the primary contact between Investigational Sites, Novotech and Sponsor, maintaining site relationships and coordinating regulatory compliance.

The Sydney-based role offers hybrid work arrangements and flexible hours to support work-life balance while delivering high-quality clinical trial monitoring and site management

Formación

• Graduate in a clinical or life sciences-related field.
• Experience in research/pharmaceutical industry or related field per job level.
• Must have full unrestricted working rights in Australia; sponsorship not provided.

Responsabilidades

• Build relationships with Principal Investigators, study coordinators, pharmacists and trial personnel to ensure efficient trial management.
• Foster internal and external stakeholder relationships to support timely project delivery.
• Collaborate with IHCRA and RSA to prepare site essential documents and support ethics/regulatory submissions.
• Understand local and international regulatory requirements related to clinical trials.
• Oversee site recruitment and engagement, and develop site-specific recruitment plans.
• Monitor investigational sites across all phases, on-site or remote as required.

Conocimientos

Site relationship management

Time management

Attention to detail

Computer literate

Educación

Bachelor's degree in clinical or life sciences

Descripción del empleo

Novotech is seeking a Clinical Research Associate (CRA) to safeguard trial participant welfare and ensure accurate, verifiable data across source documents. The CRA acts as the primary contact between Investigational Sites, Novotech and Sponsor, maintaining site relationships and coordinating regulatory compliance.

The Sydney-based role offers hybrid work arrangements and flexible hours to support work-life balance while delivering high-quality clinical trial monitoring and site management