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    Clinical Research Associate - Adelaide, Australia - I-Pharm Consulting

    I-Pharm Consulting
    I-Pharm Consulting Adelaide, Australia

    5 days ago

    Default job background
    Full time
    Description

    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 - / , or apply direct here.

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