
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
đ„ 0 minutes ago
đŠđș Australia â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ„ Clinical Operations
đ» Ghost score 10%
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Monitor performance through close interaction with project and functional leadership âą Ensure project documentation and correspondence are accurate and complete âą Serve as a senior-level project team contributor and deliver high-quality, timely work âą Generate study-specific status reports for study teams, sponsors, and/or management âą Attend project team meetings as required âą Provide consultation, facilitate metrics collection, and develop action plans to keep projects on time and within budget âą Manage and oversee team activities, including resourcing, staff assignments, quality control, and delivery efficiency âą Produce resourcing plans and monitor resource needs where assigned âą Liaise with project teams, sponsors, and management regarding direct-report performance âą Provide technical support, training, mentoring, and performance development for staff âą Conduct quality checks of deliverables and take remedial action when needed âą Participate in staff performance and salary reviews âą Support business development, client networking, public speaking, bids, and client presentations where appropriate âą Coordinate client or account activities where appropriate âą Champion Parexel and departmental systems and standards improvements âą Maintain productivity/billability and staff turnover levels âą Complete administrative tasks including timesheets, training, and travel expense claims âą Travel as needed âą Build a positive, results-oriented work environment and model teamwork âą Demonstrate leadership within the department, function, or location âą Ensure adherence to corporate policies and applicable clinical research standards
âą Demonstrated ability to manage and motivate direct reports âą Competent in local language and written English âą Oral English competency is preferred âą Substantial monitoring/data management experience or equivalent experience in clinical research âą Strong understanding and knowledge of the clinical trials environment âą Interstate travel is expected to attend meetings and assessment visits âą Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or relevant clinical other equivalent experience âą Working knowledge of and compliance with applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, Parexel SOPs, and where applicable, sponsor SOPs
Apply Nowđ August 6
Clinical Project Manager leading complex, compliant clinical trials for biopharmaceutical companies in Australia. Managing sponsors, vendors, budgets, risks, and Trial Master File documentation from start-up through closeout.