Clinical Research Associate

Opportunity to join a leading Clinical Research Organisation who are seeking experienced CRA's to join on a full-time, permanent basis in Adelaide.

You will be joining their core team and thus be partnered with a range of Pharmaceutical & Biotech sponsors, working on oncology, cardiology, neurology and other therapeutic areas (phases I-III).

Being a part of the core team will offer you a huge variety of project scope, seen as extremely valuable when looking to progress onto Clinical Project Management, having developed a robust skillset.

They also have a dedicated training programme in place for CRAs to progress onto CTM/CPM positions and promote healthy growth.

• Position: Clinical Research Associate
• Location: Adelaide, Australia

Responsibilities:

• Conduct site initiation, monitoring, and close-out visits for clinical trials in accordance with protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Ensure compliance with study protocols, investigational product accountability, and regulatory documentation.
• Build and maintain strong relationships with investigational sites, investigators, and study coordinators.
• Perform site feasibility assessments and contribute to site selection activities.
• Monitor study progress, identify potential issues, and implement corrective actions as needed.
• Assist in the preparation and review of study-related documents and reports.

Qualifications:

• Bachelor's degree in Life Sciences or related field.
• Previous experience as a Clinical Research Associate or similar role preferred.
• Knowledge of clinical research regulations and guidelines (ICH-GCP).
• Excellent communication, organisational, and problem-solving skills.
• Ability to work independently and collaborate effectively with cross-functional teams.
• Willingness to travel to investigational sites as required.

Please contact Keeley Munday on kmunday@i-pharmconsulting.com / 02 8310 5854, or apply direct here.