Site Operations Manager

Job Title: Site Operations ManagerLocation: Melbourne, Australia Company OverviewWe are partnering with one of Australia's leading Clinical Trial Networks, dedicated to conducting groundbreaking clinical trials that advance medical knowledge and patient care. With state-of-the-art facilities and a strong commitment to innovation, they offer leading project scopes across phases I-IV in diverse therapeutic areas. You will be joining a growing site in Melbourne with state-of-the-art facilities in a new private hospital. This role is perfect for an experienced coordinator, who likes to be hands on. Understands the operational side to clinical trials and is able to grow and manage a team. You will be working alongside the site director and other site managers across the Australian business - attending events together and networking across the sector. Must have a nursing background. Culture and BenefitsThe company prioritises a people-centric culture, ensuring a collaborative and friendly approach to business.They're a growing business and so offers a lot of progression opportunities for those joining. Key Responsibilities:Plan and execute clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.Work closely with investigators, study teams, sponsors, and healthcare staff to ensure smooth trial operations.Prepare and submit applications to ethics committees and governance bodies, ensuring compliance with relevant standards.Manage recruitment, informed consent processes, scheduling, and monitoring of participants' progress.Maintain accurate trial records, prepare reports for stakeholders, and ensure documentation meets audit standards.Monitor timelines, budgets, milestones, and project deliverables effectively.Ensure all aspects of the trial meet high-quality standards, including data integrity and participant safety.Provide support and guidance to site staff on protocol delivery and trial procedures. Qualifications & Experience:Nursing backgroundGood Clinical Practice (GCP) certification is highly desirable to ensure compliance with ethical and regulatory standards.Experience coordinating clinical trials across various phases (4 years) Knowledge & Skills:Strong understanding of clinical research processes and regulatory requirements.Excellent organizational and communication skills.Ability to multitask, prioritize, and work well under pressure.Attention to detail and commitment to data integrity.Proficiency in electronic data capture systems and clinical trial management software. Why Join?This is a unique opportunity to contribute to innovative clinical trials in a supportive and forward-thinking environment. Our client offers a competitive salary, professional development opportunities, and the chance to work on cutting-edge research that has a real impact on patient outcomes. How to Apply:If you are an experienced clinical professional with a passion for clinical research and are ready to take on a challenging role in clinical trial coordination, we encourage you to apply.Be a part of pioneering research and contribute to the future of medicine.