Are you a Clinical Research Associate (CRA) with 2 years 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 limited positions available for CRA 2 and Sr CRA 1 positions that we can consider 482 Sponsorship. Our ideal candidate will have 2-4 years independent monitoring experience.
Sydney and Melbourne are our preferred locations for these roles, 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 plansProvide monitoring visits and site management for a variety of protocols, sites and therapeutic areasAdminister protocol and related study training to assigned sites and establish regular lines of communicationEvaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulationsManage 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 plansCollaborate 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 essentialMinimum of 2 years independent site monitoring experience for a CRA 2 and 4 years to be considered a Sr CRA 1CRO experience is highly desiredAbility to travel on a regular basis which will involve interstate travelExtensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is requiredIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com