临床医学经理 - Shanghai

The medical writing manager is responsible for creating high-quality written content in English and Chinese. They will work with colleagues and customers to communicate effectively and integrate data from various sources. · In-depth knowledge of clinical study reports, protocols, ...

The Medical Manager will be responsible for the medical and scientific activities of assigned product(s) or tasks. They will support the development and execution of medical strategy and medical plans to optimize assigned product(s) value. · ...

This position is responsible for managing clinical trials from start to finish. The successful candidate will oversee project implementation, ensure quality control, and meet budget and timeline requirements. · Manage clinical trials from setup to closeout. · Ensure all project a ...

The Clinical Project Manager oversees clinical trials procedures from start to finish. They ensure all project activities adhere to SOPs and applicable regulations. · Review meeting minutes · Assure projects are completed within budget and schedule · Determine cause of project ov ...

This position comes from Lianjia. The job requires a bachelor's degree or above and has 3 years of medical surveillance experience. · homebased · English workable · Tumor project experience. · ...

+Job summary · The position involves leading clinical projects at Thermo Fisher Scientific. The role requires strong project management skills, ability to communicate effectively with customers and team members. · +QualificationsBachelor's degree or equivalent required. · +Skills ...

This position involves managing business related to clinical pharmacology section of clinical trial projects, · analyzing data from these sections, consulting sponsors on issues related to these sectors. · Responsible for participating in project as head of clinical pharmacology ...

The Clinical Quality Control Manager will accelerate the improvement of study quality by implementing Quality Control (QC) activities and driving quality initiatives. They will ensure clinical studies are conducted in compliance with ICH-GCP and Chinese GCP. · ...

The Clinical Quality Control Manager position involves accelerating study quality by implementing QC activities and driving quality initiatives in compliance with ICH-GCP, · Chinese GCP, · and other related Chinese regulations. · This role requires a Bachelor degree or above in M ...

This position oversees the business of the clinical pharmacology section of clinical trial projects, analyzing data and communicating consultation replies. It requires a master's degree in pharmacology-related fields, at least 7 years of experience in clinical trials, and profici ...

该职位来源于猎聘 职责描述: Broad Area-1: Medical Content Writing (Complex Projects) in Simplified Chinese · Responsible for high client satisfaction for all content milestone deliverable with regard to quality and accuracy, timelines, and efforts · Use scientific expertise to develop high-qu ...

This position is responsible for managing overall study timelines, budgets and quality targets. Accountable for building, forecasting and managing the Clinical Trial Budget. · ...

This position requires managing overall study timelines, budgets, and quality targets. · Accountable for building forecasting and managing the Clinical Trial Budget. · Leads the China core study team manages facilitates and documents core study team meetings. · ...

This position is responsible for managing overall study timelines, budgets and quality targets. The Senior Clinical Program Manager will lead the China core study team; manages, facilitates and documents core study team meetings (e.g. meeting agendas & minutes, action logs and de ...

This position is responsible for managing overall study timelines, budgets and quality targets. Accountable for building, forecasting and managing the Clinical Trial Budget. · Fosters optimal China study team health including formal team effectiveness assessments and action plann ...

The case manager will serve as a single point of contact for patients and their families. · Manage all aspects of new and existing patient queries and needs. · Ccoordinate service needs to be provided including but not limited to arrange resources set schedule transportation esco ...

该职位来源于猎聘 Key Responsibilities: Oversee end-to-end clinical trial delivery, ensuring all milestones meet on schedule and within budget, via planning, organizing, and executing. Lead and coordinate cross-functional teams including medical, site management, data management, biostati ...

This role involves developing strategic medical plans for compounds and providing medical expertise for regulatory affairs. It also includes leading scientific data dissemination and collaborating with clinical teams to design and execute clinical studies. · Writing and reviewing ...

The Job entails the following but not limited to: · Achieve revenue goals, quarter on quarter, by converting openings with existing or new clients through developing proposals, conducting pitches, and other new business closing activities · Expand footprint in key accounts, · Col ...

Drive growth by developing Medical affairs business to achieve top line goals in assigned or break-in accounts Identifying appropriate targets and expand footprint among existing accounts and new accounts · Achieve revenue goals quarter on quarter by converting openings with exis ...

该职位来源于猎聘 Study Manager (PM role), FSP Top Global Pharma 工作地点:上海/北京office based 上海市静安区南京西路1168号中信泰富广场 北京市朝阳门北大街五矿广场B座9层 项目领域:global II/III期非肿瘤项目 招聘要求: 统招本科及以上学历,医学药学相关专业 1年以上项目管理经验背景 Global公司背景优先 英语流利 Basic purpose of the job* Accountable for the operational management of the regi ...