助理法规事务总监,标签协调员
Associate Regulatory Affairs Director, Labelling Coordinator
职位名称:高级法规事务主任,标签协调员
工作地点:英国伯克郡雷丁
工作地点类型:远程
工作合同类型:全职
职位级别:
职位概述
直接指导、监督和管理复杂的标签和法规项目,确保按时且在预算内交付高质量成果。确保所有项目工作均符合标准操作程序、政策和实践。
主要职责
• 可能作为大型独立项目的项目经理,涉及多个法规或技术交付物和/或地区和/或运营;进行风险分析、管理和应急计划;
• 为各种项目提供战略法规和/或技术咨询,内部和外部使用适当的创新解决方案;
• 可能与监管机构召开会议;
• 可能撰写和/或审核完整的单一服务法规提案,并向客户说明成本和时间线;
• 为初级同事提供指导,并就多种法规文件类型提供建议;
• 可能策划并就标签/法规事务主题在会议或出版物中进行研讨会或演讲;
• 可能被指定为法规标准操作程序或由其他运营部门拥有的跨职能标准操作程序的审核人和/或批准人;
• 可能支持全球法规或技术倡议,或担任专业领域专家。
• 执行法规管理分配的其他任务或任务;
资格要求
• 生命科学或相关学科学士学位 或
• 生命科学或相关学科硕士学位
• 至少12年相关经验,包括8年标签法规经验或教育、培训和经验的组合
• 在欧盟标签更新提交方面有丰富经验
• 具备高级谈判和影响能力,能够识别和解决问题,采用灵活适应的方法。在与客户的挑战性互动中保持冷静、坚定和外交风格
• 熟练掌握软件和计算机技能,包括MS Office应用
• 为初级同事树立榜样;具备积极的态度和与客户及同事的沟通风格。能够有效与组织各层级沟通,在变化和其他压力情况下保持积极和热情
• 能力
查看英文原文
Job Title: Associate Regulatory Affairs Director, Labelling Coordinator
Job Location: Reading, Berkshire, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Job Overview
Direct, oversee and manage complex labeling and regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is completed in accordance with standard operating procedures, policies and practices.
Essential Functions
• May act as a Project Manager for a large stand-alone program, involving several regulatory or technical deliverables and/or region, and/or operation; Undertakes risk analysis, management and contingency plans, as appropriate;
• Provides strategic regulatory and/or technical consultancy on a variety of projects, internally and externally, using innovative solutions where appropriate;
• May manage meetings with Regulatory Agencies;
• May write and/or review a complete single service regulatory proposal and defend costs and timelines to clients;
• Provides mentorship to junior colleagues and advise others on many regulatory document types;
• May plan and deliver workshops or presentations on Labeling / Regulatory Affairs topics for conferences or publications;
• May be assigned as Reviewer and/or Approver for Regulatory standard operating procedures or cross-functional standard operating procedures owned by other operations;
• May support global regulatory or technical initiatives or act as a Subject Matter Expert.
• Performs other tasks or assignments, as delegated by Regulatory management;
Qualifications
• Bachelor's Degree Degree in LiveScience or related discipline Req Or
• Master's Degree Degree in Life science or related discipline
• At least 12 years relevant experience including 8 years labeling regulatory experience or combination of education, training and experience
• Extensive experience in EU labeling updates submissions
• Advanced negotiating and influencing skills and the ability to identify and resolve issues, using flexible adaptable approach. Remains calm, assertive and diplomatic in challenging interactions with customers
• Strong software and computer skills, including MS Office applications
• Acts as a role model to junior colleagues; possesses a positive attitude and communication style to customers and colleagues. Communicates effectively with all levels of the organization and remains motivated and enthusiastic in times of change and other pressure situations
• Ability to exercise independent judgement taking calculated risks when making decisions
• Applicable certifications and licenses as required by country, state, and/or other regulatory bodies
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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Originally posted on Himalayas