Clinical Project Assistant

Job not on LinkedIn

🔥 38 minutes ago

🇦🇺 Australia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Assistant

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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GenesisCare

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

🏥 Healthcare

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 Private Equity Round on 2018-10

Healthcare • Healthcare Insurance • Pharmaceuticals

GenesisCare is a healthcare provider that specializes in oncology, offering personalized cancer treatments and diagnostic services. They provide world-class cancer care, including advanced treatments such as radiotherapy, chemotherapy, immunotherapy, and theranostics. GenesisCare is dedicated to improving patient experiences and outcomes in cancer care, with facilities worldwide and ongoing research in clinical trials.

📋 Description

• Support Project Managers and project teams with the coordination of clinical research studies • Prepare, collect and maintain study documentation throughout the project lifecycle • Support the setup and maintenance of Trial Master Files and electronic Trial Master Files • Assist with project tracking, reporting, forecasting and invoicing activities • Maintain project training records, databases and Clinical Trial Management Systems • Coordinate project meetings, agendas, minutes and follow-up activities • Assist with study materials, investigator meetings and project communications • Support the tracking of project metrics and help identify opportunities to improve processes • Work collaboratively with colleagues across Clinical Operations, Data Management, Clinical Research and Quality • Help ensure project documentation is accurate, current and maintained in line with study and regulatory requirements

🎯 Requirements

• Hold a qualification in Life Sciences, such as Biology, Chemistry, Pharmaceuticals or a related discipline • Have experience working within a clinical research environment • Have an understanding of clinical research processes and ICH GCP requirements • Have experience with CTMS or electronic Trial Master File systems, which would be advantageous • Are highly organised and able to manage competing priorities and deadlines • Communicate clearly and confidently, both verbally and in writing • Are proactive, detail focused and comfortable taking ownership of your work • Are confident working independently while staying connected to a virtual team • Can collaborate effectively with stakeholders across multidisciplinary project teams • Certain roles may require evidence of vaccination against or non-susceptibility to specified vaccine preventable diseases

🏖️ Benefits

• Enjoy the flexibility of working remotely • Build your clinical research and project coordination experience • Gain exposure across different stages of the clinical research lifecycle • Work alongside experienced Project Managers and clinical research professionals • Develop your knowledge of clinical trial systems, documentation and project operations • Join a collaborative team where you can continue learning and developing your career • Contribute to meaningful clinical research that ultimately supports better patient outcomes