出海雷达

Associate Director, Regulatory Affairs - UK & Ireland

其他限定地区(需当地身份)日间重叠仅 1 小时,需熬夜配合
公司BeiGene
薪资£80,700 - £100,900/年
工作地点United Kingdom
地域资格限定地区(需当地身份)
时区要求日间重叠仅 1 小时,需熬夜配合
用工类型Full Time
发布时间今天
数据来源Himalayas
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注意地域限制:该职位明确限定在 United Kingdom 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:日间重叠仅 1 小时,需熬夜配合。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

贝继续以快速的速度发展,为经验丰富专业人员提供了挑战性和令人兴奋的机会。在考虑候选人时,我们寻找具有高度动机,协作能力,最重要的是,与癌症斗争激情共享的科学和商业专业人士。一般描述:监管事务副主任将负责制定和实施英国开发方案的监管战略,以确保并保持产品销售许可 (如同企业目标),并在与关键内部利益相关者协调下。这将包括对英国和爱尔兰的商业产品的监督和管理。工作的主要功能:该个人将领导英国 RA 团队通过以下详细说明,在产品开发,注册,批准后以及生命周期的所有阶段管理指定化合物的监管方面 (NME/新指标): ·与关键内部利益相关者合作确定英国 MAA 战略并确保监管策略是按照产品发展目标纳入和实施的 ·管理监管文件内容和准备。了解欧盟 MAA 文件的内容,以支持标签更新和管理在爱尔兰确保遵守英国和爱尔兰监管要求。监督并负责监管机构的通信,提交和批准,专注于质量,以确保第一轮/试验审批 ·审查和提供促进材料对英国和爱爾兰 ·作为英国领导团队中的 RA 联系人,参加定期会议并为英国商业战略提供意见 ·为 HA 互动做好团队准备,并进行中级和领导讨论,成为 MHRA 对战略性非研究具体话题的主要联系人,并为欧盟 RA 团队提供与卫生当局相关的临床问题方面的支持。·积极预测和缓解监管风险,同时保持有关监管情报,程序,变化和趋势的当前知识。·提供提交差距分析,确定潜在风险,提出潜在解决方案/减轻计划以确保提交成功接受。·确保符合欧盟/英国全球监管要求。·指导和辅导小组成员。代表 BeOne 在英国工业协会会议和大会上监督 R

查看英文原文

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.
General Description:
The Associate Director of Regulatory Affairs will be responsible for developing and implementing UK regulatory strategies for development programs to secure and maintain the marketing authorization for product(s) in line with business objectives, and in coordination with key internal stakeholders. This will also include oversight and management of commercial products for both UK and Ireland.
Essential Functions of the job:
This individual will lead the UK RA team to manage regulatory aspects of designated compounds (NME/New indications) through all phases of development, registration, post-approval, and lifecycle of the product as detailed below:

  • Collaborate with key internal stakeholders to define UK MAA strategy and ensure the regulatory strategy is incorporated and implemented in line with product development objectives
  • Manage the content of and prepare regulatory (UK MAA) dossiers. Have knowledge of the content of the EU MAA dossiers to support labeling updates and management in Ireland ensuring compliance with UK and Ireland regulatory requirements. Oversee and be accountable for regulatory agency communications, submissions, and approvals, with a quality focus to secure first-cycle/attempt approvals
  • Review and provide input into promotional materials for both UK and Ireland
  • Act as the RA liaison within the UK Leadership team, attend regular meetings and provide input into UK business strategy
  • Prepare team for HA interactions, and moderate and lead discussions, be the main MHRA contact for strategic, non-study specific topics and provide support to the EU RA team for clinical matters related to Health Authority topics.
  • Proactively anticipate and mitigate regulatory risks while maintaining current knowledge of regulatory intelligence, procedures, changes, and trends.
  • Provide submission gap analyses, identify potential risks and propose potential solutions/mitigation plans to ensure successful acceptance of submissions.
  • Ensure compliance with EU/UK global regulatory requirements.
  • To lead and mentor junior team members.
  • Represent BeOne at UK industrial association meetings and congresses

Supervisory Responsibilities:
· Junior Regulatory Affairs professionals
Computer Skills: Extensive experience with Microsoft Office suite, Veeva regulatory publishing and expertise with PowerPoint presentation authoring and presentation.
Education Required:
Bachelor’s degree required; advanced degree preferred.
Other Qualifications:
· Minimum of 8 years’ experience in the biotechnical or pharmaceutical industry, and a minimum of 8 years’ experience in a Regulatory capacity with a broad background.
· Experience working with MHRA regulatory procedures is mandatory for this role.
· Sound understanding of the drug development process, the pharmaceutical industry and healthcare environment including UK regulatory requirements and policy trends
· Recent experience with oncology products and MAAs, ODD, PIP is preferred
· Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism
Location: UK, fully remote
Travel: Travel to internal meetings in UK monthly or bimonthly. Additional travel to EU locations occasionally
Salary Range UK: 80,700.00 GBP - 100,900.00 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

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