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高级全球临床流程管理专员

雇主

BeiGene

地点

远程 · Remote · 英国

待遇

£GBP 43,400 - GBP 54,200 / annual

工作模式

远程

截止日期

1月6日

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岗位摘要

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.

岗位职责

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
The role provides coordination and operational support to Process Leads and senior GCPM leadership to enable effective execution of process management activities, document control workflows, governance alignment, status oversight, and intake-driven insights. The incumbent supports the preparation, organization, analysis, and tracking of key inputs, project plans, stakeholder materials, approval activities, reporting outputs, and GCPM intake data to facilitate timely decision-making, process progression, continuous improvement, innovation consideration, and consistent delivery of GCPM-owned initiatives.
Responsibilities:
Coordination Support to Process Leads
Support document review and approval workflows to enable timely progression, system/document governance, and completion of required approval steps.
Coordinate document control activities, including initiating Document Control engagement, supporting QA alignment, submitting and facilitating DCC activities, and tracking approvals through completion.
Support information gathering, preparation, tabulation, and organization of inputs to enable efficient Process Lead review and decision-making.
Assist with the development, documentation, and maintenance of project plans, including regular status reviews, updates, and follow-up on outstanding information.
Support the creation and maintenance of stakeholder lists, meeting planning materials, and project charter drafts.
Provide administrative support for organizational change management activities, including preparing draft communications under Business Owner and Process Owner guidance.
Coordination Support to Senior Manager
Compile data from Veeva Vault or equivalent source systems to support status reporting and periodic review of processes under GCPM leadership.
Prepare and maintain QE CAPA tables and related tracking materials for periodic review by the Senior Manager and Head of GCPM.
Prepare and analyze data from the GCPM intake form to support management review, process improvement planning, and evaluation of potential innovation opportunities.
Computer Skills:Efficient in Microsoft suite (Excel, Outlook, Word, PowerPoint, Project)
Other Qualifications:
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)
Supervisory Responsibilities:No
Salary Range UK:43,400.00 GBP - 54,200.00 GBP
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
Originally posted on Himalayas

申请条件

- 具有科学或商业专业背景
- 高度积极主动
- 具备协作能力
- 对抗击癌症有强烈兴趣和热情
- 有相关领域工作经验
- 具备协调和运营支持能力
- 能够支持文件审查和审批流程
- 熟悉文件控制活动
- 具备信息收集、整理和制表能力
- 能够协助制定和维护项目计划
- 具备利益相关者列表和会议材料准备能力
- 能够提供组织变革管理的行政支持
- 熟悉Veeva Vault或类似系统
- 具备数据汇编和分析能力
- 能够跟踪审批流程直至完成
- 具备支持及时决策和流程推进的能力
- 能够促进持续改进和创新考量

雇主简介

BeiGene is a global, science-driven biopharmaceutical company focused on developing innovative medicines for cancer and expanding into immunology and inflammation therapies.

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数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有