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Form of work IQVIA Australia
Are you a Clinical Research Associate or Senior Clinical Research Associate looking for a new and exciting challenge with opportunity for ongoing support and growth? Are you looking for a career and not just a job? Then we have the role for you!
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 enrolment, 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
$95,000 - $148,600 salary package + super
https://www.iqvia.com/locations/australia-and-new-zealandthe way. Learn more at jobs.iqvia.com.
