Are you looking for a challenging role as a Clinical Research Associate? We have exciting opportunities for experienced CRAs to join our team in Sydney and Melbourne.
Your key responsibilities will include site selection, initiation, monitoring, and close-out visits. You will work with sites to adapt, drive, and track subject recruitment plans. You will also provide monitoring visits and site management for various protocols, sites, and therapeutic areas.
We are seeking highly skilled individuals with a minimum of 2 years independent site monitoring experience for CRA 2 positions and 4 years for Sr CRA 1 positions. You must have a Bachelor's degree in Life Sciences or other scientific/nursing disciplines. CRO experience is highly desirable, and extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is required.
You will be responsible for administering protocol and related study training to assigned sites and establishing regular lines of communication. You will evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. You will 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.
* Suitable candidates will have:
* Bachelor's degree in Life Sciences or other scientific/nursing disciplines
* Minimum of 2 years independent site monitoring experience for CRA 2 and 4 years for Sr CRA 1
* CRO experience is highly desired
* Ability to travel on a regular basis, including interstate travel
* Extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines