Clinical Research Associate 2

vor 1 Monat

Perth, Österreich Iqvia Argentina Vollzeit

Are you a Clinical Research Associate (CRA) with 2 years of independent monitoring experience?
Have you always wanted to live and work abroad?
Has coming to Australia always been on your bucket list?
Want to try something different in 2025?
We currently have 4 new CRA 2 level positions that we can consider for 482 Sponsorship.
At this stage, we will not be seeking Senior level appointments.
Sydney and Melbourne are our preferred locations for these roles, and prior Oncology experience is also a must-have to proceed to interview.
As part of the interview process, you will be expected to complete a video assessment.
Only successful candidates will be notified.
Key Responsibilities

Perform site selection, initiation, monitoring, and close-out visits and work with sites to adapt, drive, and track subject recruitment plans.
Provide monitoring visits and site management for a variety of protocols, sites, and therapeutic areas.
Administer protocol and related study training to assigned sites and establish regular lines of communication.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans.
Collaborate and liaise with study team members for project execution support as appropriate.

Not everyone can be a CRA; it's an extraordinary role.
Do you meet this unique criteria?

Bachelor's degree in Life Sciences or other scientific/nursing disciplines is essential.
Minimum of 2 years independent site monitoring experience.
CRO experience is highly desired.
Ability to travel on a regular basis which will involve interstate travel.
Extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is required.

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