Senior Clinical Trials Coordinator

Sydney Clinical Trials Pty Ltd; Campbelltown; Presencial; AUD 70.000 - 90.000; A tiempo parcial

Descripción de la vacante

Sydney Clinical Trials Pty Ltd is seeking an experienced Clinical Trials Coordinator for a casual role up to 40 hours per week at Campbelltown NSW. The successful candidate will coordinate trials from start-up to close-out, ensuring adherence to GCP, ICH guidelines, and study protocols, while maintaining high-quality data and participant care.

Responsibilities include participant recruitment, data entry into EDC/CTMS, and assisting with audits.

Formación

• 2+ years coordinating sponsor-initiated pharma clinical trials in healthcare settings.
• Strong knowledge of ICH-GCP guidelines, trial regulations and ethics requirements.
• Experience across Phase I–IV trials; gastroenterology/hepatic areas beneficial.

Responsabilidades

• Coordinate all aspects of clinical trial activities from start-up through close-out.
• Manage participant recruitment, screening, follow-up visits, bookings, sample processing and shipment.
• Ensure compliance with study protocols, GCP and ICH guidelines.
• Prepare and maintain accurate trial documentation, source documents, and investigator site files.
• Enter study data into EDC systems and CTMS; track adverse events and report per protocol.
• Coordinate investigational product accountability and study-related supplies.
• Support audit and inspection readiness activities.
• Maintain confidentiality and safeguard participant data at all times.

Conocimientos

Participant care

Organisational skills

Communication skills

Problem-solving

Attention to detail

Time management

Multitasking

Collaboration

Independence

Educación

Health Science / Life Science / Nursing degree

Herramientas

CTMS

EDC systems

Descripción del empleo

Sydney Clinical Trials Pty Ltd is seeking an experienced Clinical Trials Coordinator for a casual role up to 40 hours per week at Campbelltown NSW. The successful candidate will coordinate trials from start-up to close-out, ensuring adherence to GCP, ICH guidelines, and study protocols, while maintaining high-quality data and participant care.

Responsibilities include participant recruitment, data entry into EDC/CTMS, and assisting with audits.