About this role
ProPharma has improved patient health for 20 years by empowering biotech, med device, and pharmaceutical organizations to advance breakthroughs and introduce therapies. We seek a motivated, detail-oriented Clinical Research Associate for a flexible 0.2 FTE role. Contribute to high-quality clinical research projects while enjoying part-time work.
Conduct site monitoring visits remotely and on-site per study protocols, ICH-GCP, and regulations. Ensure data integrity through source data verification and support site activities from initiation to close-out. Build strong relationships with investigational sites and collaborate with cross-functional teams.
Work in a partner-focused environment with deep expertise in regulatory sciences, clinical research, quality, pharmacovigilance, and R&D technology. Hybrid model encouraged for those near offices to foster in-person collaboration. All roles treated on merit regardless of location proximity.
Join a diverse, inclusive workplace committed to equity where employees unleash innovative spirits. Applications personally reviewed by recruitment team without AI screening. Receive an outcome on every application to know your status.
Requirements
- Previous experience as a Clinical Research Associate (or similar role)
- Strong understanding of ICH-GCP guidelines and clinical trial processes
- Excellent communication and organisational skills
- Ability to work independently with minimal supervision
- Located in NSW or Melbourne, with willingness to travel occasionally if required
- Relevant degree in life sciences, nursing, or a related field preferred
Responsibilities
- Conduct site monitoring visits (remote and on-site as required) in accordance with study protocols, ICH-GCP, and regulatory requirements
- Ensure data integrity and compliance through source data verification (SDV)
- Build and maintain strong relationships with investigational sites
- Support site initiation, monitoring, and close-out activities
- Identify and escalate risks or issues impacting study delivery
- Assist with regulatory document review and maintenance of Trial Master Files (TMF)
- Collaborate with cross-functional teams to ensure smooth study execution
Benefits
- 0.2 FTE flexible part-time schedule (one day per week equivalent)
- Hybrid working option encouraged near offices for collaboration
- Commitment to diversity, equity, and inclusion as an Equal Opportunity Employer
- All applications personally reviewed by recruitment team, no AI screening
- Guaranteed outcome response on every application
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