On-Site Clinical Trial Coordinator for Patient-Centered Studies

AIM Research; Newcastle City Council; Presencial; AUD 70 000 - 100 000; Tempo integral

Resumo da oferta

AIM Research is seeking a Clinical Trial Coordinator for a full-time, on-site role in the Greater Newcastle Area. You will coordinate day-to-day trial activities, support protocol implementation, and ensure data integrity.

Responsibilities include scheduling, documentation, ethics submissions, and cross-functional communication with investigators, sponsors, and participants. A background in clinical research and strong organizational skills are essential.

Qualificações

• Clinical research expertise to support high-quality study conduct.
• Understanding of study Protocols and GCP-aligned procedures.
• Strong project management and coordination skills.
• Excellent communication with participants, investigators, sponsors, and teams.
• Attention to detail and meticulous data documentation.
• Ability to work in a fast-paced clinical environment.

Responsabilidades

• Coordinate day-to-day clinical trial activities and visit scheduling.
• Maintain accurate study documentation and records in a timely manner.
• Support protocol implementation and ethics/regulatory submissions.
• Monitor data quality, timelines, and milestones; ensure GCP compliance.
• Facilitate communication among clinicians, sponsors, and participants.
• Assist with screening, enrollment, and preparation of study materials.

Conhecimentos

Clinical research

Regulatory knowledge

Project coordination

Communication skills

Attention to detail

Organizational skills

EDC systems

Data entry accuracy

Ferramentas

EDC systems

Office software

Descrição da oferta de emprego

AIM Research is seeking a Clinical Trial Coordinator for a full-time, on-site role in the Greater Newcastle Area. You will coordinate day-to-day trial activities, support protocol implementation, and ensure data integrity.

Responsibilities include scheduling, documentation, ethics submissions, and cross-functional communication with investigators, sponsors, and participants. A background in clinical research and strong organizational skills are essential.