高级医学总监
Senior Medical Director
工作时间
标准（周一至周五）
工作环境
办公室
职位描述
作为Thermo Fisher Scientific团队的一员，您将从事具有深远意义的工作，在全球范围内产生积极影响。与我们的同事一起，每天实现我们的使命，帮助客户让世界更健康、更清洁、更安全。我们为全球团队提供实现个人职业目标所需的资源，同时通过开发解决世界上最严峻挑战的解决方案，如保护环境、确保食品安全或帮助找到癌症的治疗方法，推动科学向前发展。
由于持续增长，CRG现在正在寻找一名助理医学总监/神经科学医学总监，加入我们在中国的医学总监团队。该职位可以是办公地点或居家办公。
助理医学总监/医学总监将负责为PPD药物警戒部门内的临床试验和安全性评估提供医学支持和医学建议。
日常工作内容：
- 提供针对研究、项目和计划的医学监测和审查服务，包括但不限于：
- 领导合同任务的所有医学方面。监督安全变量。
- 与客户、研究者和医疗专业人员讨论医学问题，在审批前和审批后服务中运用准确的医学判断、解释和决策。
- 为团队成员提供医学咨询，解答与研究相关的医学问题。与同事和客户进行清晰沟通，保持开放的沟通渠道，确保所有程序得到适当执行。
- 分析和评估安全数据，识别并处理新兴的安全信号。
- 医学审查个例安全报告、严重不良事件报告和临床结果报告。
- 协助业务拓展活动
- 在业务拓展会议中向客户展示PPD的标准医学安全流程，并与各种医学社区建立联系，探索和扩展PPD业务。
- 参与项目团队的培训。
- 根据需要提供治疗领域和方案培训。
- 编写、审查和批准报告、监管提交文件和方案，确保医学内容准确完整。
最初发布于Himalayas
查看英文原文
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Due to continued growth, CRG is now looking to appoint an Associate Medical Director/Medical Director of Neuroscience, to join our team of Medical Directors in China. This role can be office-based or home based.
The Associate Medical Director/Medical Director will be responsible for providing medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
A day in the Life:
- Provide study, project and program-specific medical monitoring and review services, including but not restricted to:
- Leading of all medical aspects of contracted tasks. Supervising of safety variables.
- Discussing with clients, investigators and healthcare professionals of medical issues in the pre and post approval services by using accurate medical judgment, interpretation and decision.
- Provide medical consultation to team members and answer study related medical questions. Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately
- Analysis and assessment of safety data to identify and run emerging safety signals.
- Medical review of individual case safety reports, serious adverse event reports and clinical outcome reports.
- Assist in Business Development activities
- Present PPD standard medical safety processes to clients at business development meetings and connect with various medical communities to explore and expand PPD business.
- Participate in training of project teams.
- Provide therapeutic and protocol training as needed.
- Write, review and approve reports, regulatory submissions and protocols, ensuring that the medical content is accurate and complete.
Originally posted on Himalayas