Senior Global Clinical Process Management Specialist

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

💵 £43.4k - £54.2k / year

⏰ Full Time

🟠 Senior

👻 Ghost score 0%

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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

• Provide coordination and operational support to Process Leads and senior GCPM leadership • Support document review and approval workflows, document control activities, QA alignment, DCC activities, and approval tracking • Gather, prepare, tabulate, and organize inputs for Process Lead review and decision-making • Develop, document, and maintain project plans, including status reviews and follow-up • Create and maintain stakeholder lists, meeting planning materials, and project charter drafts • Provide administrative support for organizational change management activities and draft communications • Compile data from Veeva Vault or equivalent systems for status reporting and periodic process reviews • Prepare and maintain QE CAPA tables and related tracking materials • Prepare and analyze GCPM intake data for management review, process improvement planning, and innovation evaluation

🎯 Requirements

• Efficient in Microsoft suite (Excel, Outlook, Word, PowerPoint, Project) • Fluent English (Oral; Written) • Minimum of 2 years of experience in pharmaceutical and/or biotechnology sector • Knowledge of ICH-GCP • Excellent interpersonal and problem-solving skills • Excellent organizational skills and a pre-disposition to quality management and process improvement • Effective communicator (oral and written) • Willingness to support document control, governance, and approval workflows • No supervisory responsibilities