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Form of workIQVIA 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.
