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The Senior Site Activation Specialist will execute site activation activities, prepare site documentation, review contracts, and collaborate with teams to manage site performance. The role involves tracking document progress and maintaining timelines within a sponsor-dedicated team. It requires a minimum of 3 years of relevant experience in clinical research and healthcare environments, along with a Bachelor's degree in Life Sciences or related field.

The Site Activation Specialist will manage and execute feasibility, site identification, regulatory, start-up, and maintenance activities for clinical trials. This role involves preparing and managing site documents, collaborating with teams to ensure compliance, and tracking document progress.

The Senior Site Contract Manager will negotiate clinical agreements and budgets, prepare contract templates, and advise study teams and sponsors. This role requires a strong understanding of clinical research and site start-up operations in Australia/New Zealand, with a focus on communication and organizational skills.