Clinical Research Associate

If you're looking to progress, this role is for you!
Chance to join a developing CRO in Melbourne, Australia!
This company have seen huge successes in recent years and so have some ambitious growth plans to double in size.
That means anyone joining now will be in a strong position to upskill and develop as the teams start to grow - likely to move to leadership roles in the coming years.
Culture is at the forefront for this organisation, and ensuring the teams continue to have close-knit and collaborative environments will remain a focus throughout their growth.
CRA ICRA IISenior CRAThis role would suit anyone with at least 12-months independent monitoring experience across Australian sites.
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 at a CRO or Pharma.Knowledge of clinical research regulations and guidelines (ICH-GCP).Willingness to travel to investigational sites as required.Title: Clinical Research Associate (CRA) I, II or Senior (depending on experience level)
Location: Melbourne, Australia
Salary: Market salary - open to negotiate
Please contact Keeley Munday on / or apply direct here.
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