Description:
Clinical Research Associate II / Senior CRA
Location: Melbourne
Join a collaborative team as a Clinical Research Associate II or Senior CRA, supporting a portfolio of biotech clinical trials. This role involves working on complex studies, primarily in oncology, respiratory, and related therapeutic areas, alongside leading investigators and sponsor representatives.
This is a growing team AND a growing company and so offers strong progression opportunities. This includes tailored and development programmes in place to support growth from CRA to CPM or COM.
CRA II
CRA III
Senior CRA
Must have at least 12-months experience conducting independent monitoring visits.
Key Responsibilities
- Conduct site qualification, initiation, routine monitoring, and close-out visits for biotech clinical trials.
- Ensure compliance with ICH-GCP, regulatory requirements, and study protocols throughout the study lifecycle.
- Manage site relationships, monitor data integrity, and oversee patient safety.
- Resolve data queries and contribute to clinical study documentation and reports.
- Support feasibility assessments, site activation, and patient recruitment activities.
About You
- Bachelor’s degree in life sciences or healthcare.
- At least 18 months’ independent onsite monitoring experience as a CRA256.
- Good working knowledge of clinical trial regulations (ICH-GCP, TGA, FDA).
- Strong communication, organisational, and problem-solving skills.
- Able to work autonomously and travel as required.
Why Apply?
- Defined career progression pathways, including opportunities to advance to Project Management or leadership roles.
- Involvement in innovative oncology and biotech trials with global impact.
- Flexible working arrangements and a supportive team culture.
- Access to industry-leading training and professional development.
To apply, please contact Keeley Munday at kmunday@i-pharmconsulting.com. Advance your career with a CRO where your expertise supports the development of new therapies.