We currently have a new role in our New Zealand team. We are growing and want you to be part of our success. As part of the interview process, you will be expected to complete a video assessment. Only successful candidates will be notified. This role will be based in Auckland and you are expected to travel for work from time to time within the region. 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. The right candidate for this role needs to have or demonstrate: Bachelor's degree in Sciences or other scientific/nursing disciplines, or a Minimum of 3 years relevant experience if without a degree 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 The salary range for this role is from $110,000 to $130,000 per annum with regular 38 hours of work per week, up to 40 hours if required. If this sounds like you, please apply today with your CV and a cover letter.