Clinical Trials Admin & Governance Specialist

Victorian Government; Victoria; On-site; AUD 69,000 - 77,000; Full time

Benefits offered by this job

Salary packaging up to $9,000 per year

Meals/Entertainment benefit up to $2,,

Professional development opportunities

Staff Wellbeing Centre access

Fitness Passport access

Job summary

Latrobe Regional Health in Gippsland seeks a Clinical Trials Administration Officer to support trials and teletrials on a full-time, fixed-term basis for 12 months. You will join the Research unit and provide essential governance, data management and coordination to ensure adherence to protocols and regulatory standards.

The role requires strong organisational skills and the ability to work independently within a collaborative research environment, contributing to high-quality patient care and

Qualifications

• Strong organisational and administrative skills.
• Excellent communication and interpersonal abilities.
• Ability to work autonomously within a multidisciplinary team.

Responsibilities

• Provide administrative and operational support for clinical trials and teletrials in accordance with protocols and regulatory requirements.
• Maintain accurate study files, trial documentation and records in trial management systems and databases.
• Support governance activities, including ethics submissions and regulatory documentation.
• Assist with sample handling, kit control, data entry, site monitoring visits and trial coordination.
• Build effective relationships with investigators, sponsors, staff and participants.
• Contribute to ongoing improvements of trial processes and compliance.

Skills

Organisational skills

Administrative skills

Communication skills

Autonomy

Job description

Latrobe Regional Health in Gippsland seeks a Clinical Trials Administration Officer to support trials and teletrials on a full-time, fixed-term basis for 12 months. You will join the Research unit and provide essential governance, data management and coordination to ensure adherence to protocols and regulatory standards.

The role requires strong organisational skills and the ability to work independently within a collaborative research environment, contributing to high-quality patient care and