Clinical Research Associate 2

Clinical Research Associate 2
Company:

Iqvia


Details of the offer

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? 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 a must-have to proceed to the 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.

IQVIA 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. #J-18808-Ljbffr


Source: Talent2_Ppc

Job Function:

Requirements

Clinical Research Associate 2
Company:

Iqvia


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