Neurology Clinical Trials Assistant – Impactful Research Support

Ingham Institute; Liverpool; Sur place; AUD 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

Salary packaging options

Meal Entertainment card

State-of-the-art facilities

Training and career progression

Staff wellbeing support

Gym discount

Résumé du poste

The Ingham Institute for Applied Medical Research is seeking a Clinical Trial Assistant to provide essential administrative support across a diverse portfolio of clinical research studies. You will work with investigators, research nurses and study coordinators to maintain documentation, coordinate appointments and ensure trial activities comply with regulatory requirements.

The role is a full-time (1 FTE) 12-month contract, requiring strong organisational skills, attention to detail and

Qualifications

• Current Good Clinical Practice (GCP) certification or willingness to obtain during onboarding.
• Proven administrative experience requiring high levels of organisation, accuracy and attention to detail.
• Proficiency with Microsoft Office Suite (Outlook, Word, Excel).
• Ability to maintain accurate records and manage filing systems.

Responsabilités

• Provide essential administrative support across a diverse portfolio of clinical research studies.
• Coordinate appointments, manage study records and ensure trial activities are delivered efficiently and in compliance with regulatory requirements.
• Support investigators, research nurses and study coordinators with documentation and regulatory compliance.

Connaissances

GCP certification

MS Office Suite

Communication skills

Organisational skills

Record keeping

Formation

Science/Health Science/Biomedical Science qualifications or equivalent

Outils

EDC/eMR/CTMS experience

Description du poste

The Ingham Institute for Applied Medical Research is seeking a Clinical Trial Assistant to provide essential administrative support across a diverse portfolio of clinical research studies. You will work with investigators, research nurses and study coordinators to maintain documentation, coordinate appointments and ensure trial activities comply with regulatory requirements.

The role is a full-time (1 FTE) 12-month contract, requiring strong organisational skills, attention to detail and