Senior Global Study Management Associate – Global CTA

🕒 July 14

🇦🇺 Australia – Remote

⏰ Full Time

🟠 Senior

✨ Associate

👻 Ghost score 38%

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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BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• Support the Global Clinical Study Manager in global study delivery and ensure delegated clinical study components meet quality standards, timelines, and budget • Support alignment of study goals with clinical operations objectives • Support study vendor management and other assigned study management activities • Support cross-functional Clinical Study Team meeting organization and logistics • Collaborate with Global Clinical Study Managers, Regional Clinical Trial Management Associates, and global and regional stakeholders • Support study setup and maintenance in systems such as eTMF and CTMS • Manage study-level SharePoint, distribution lists, system access, and user accounts • Support development and review of study plans and study-related documents • Organize investigator meetings and support site feasibility assessments • Track study deliverables, prepare management metrics and updates, and support study communications • Support study-level TMF creation, maintenance, document review, and quality control • Support study drug forecasting and supply activities • Support data cleaning and follow-up of outstanding information • Support planning and execution of the Clinical Study Report • Support identification and resolution of operational risks and issues • Support development of study tools, work instructions, and SOPs • Support vendor selection and setup for outsourced activities • Support study budget management, PO setup, and invoice tracking • May mentor junior team members and onboard new hires

🎯 Requirements

• Bachelor or higher degree in a scientific or healthcare discipline; higher degree preferred • Proficiency in MS Office Suite, including Excel, PowerPoint, and Project • Knowledge of clinical operations methodologies • Understanding of operational aspects of clinical study processes • 3 or more years of experience in clinical research within Biotech, Pharma or CRO industry • Limited travel might be required

🏖️ Benefits

• Market competitive compensation package including performance-based annual bonus scheme • Company shares (generous welcome grant!) • In-house and external learning and development opportunities • Fantastic benefits program • Dynamic, collaborative, supportive, inclusive, and fun team environment