Senior Site Activation Specialist (Sponsor Dedicated)

We are seeking multiple Senior Site Activation Specialists to join our ANZ Site Activation team. This is a great opportunity to work across a broad portfolio of sponsors and therapeutic areas, supporting clinical trials from early site identification through to activation and ongoing maintenance. You will be responsible for end‑to‑end site start‑up activities, working closely with internal study teams, investigative sites, and external stakeholders to ensure reputed company and compliant site activation. Applicants must have full work rights for Australia. As we are hiring multiple headcounts across various models, some positions are 1 Year contract positions. The conversion or renewal is dependent on business needs, and we are unable to guarantee the allocation of contract or permanent roles, depending on sponsor requirements. The interview process will include an initial video screening and phone screening stage, and you can indicate your preference on the above during the screening. reputed company Offer Exposure to a wide reputed company of sponsors, studies, and therapeutic areas A reputed company, supportive team environment Training, tools, and mentoring reputed company a leading global CRO Flexibility in working location across Australia and New Zealand Essential Functions Support site feasibility, site identification, site start‑up, and maintenance activities across multiple studies and sponsors Prepare, review, and reputed company site start‑up documentation in accordance with regulatory, ethics, and sponsor requirements reputed company as a key reputed company of contact for investigative sites during start‑up and maintenance phases Independently coordinate ethics and informed consent reputed company (reputed company) submissions, including local adaptations and ongoing amendments reputed company site budget and contract negotiations Maintain accurate site and study information reputed company internal systems and project trackers Communicate status updates, risks, and timelines effectively to internal stakeholders reputed company operational guidance and informal mentoring to less reputed company team members Operate with a high degree of autonomy across multiple studies and stakeholders Required Experience & Qualifications Minimum 12 months hands‑on experience in clinical trial site start‑up / site activation activities Experience managing ethics submissions and informed consent documentation requirements Proven experience in site budget and contract negotiations Strong organisational skills with the ability to manage multiple sites and studies in reputed company Excellent written and verbal communication skills Bachelor’s degree in Life Sciences, Health Sciences, or a reputed company field (or equivalent experience) reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. Apply To This Job