上海相关职位: 医疗器械注册工程师 高级客户服务工程师 分析仪器销售经理-上海 Sr/CRA(高级)临床监查员(上海) 医药销售 大区经理 学术推广专员(处方药) 市场推广专员(会务专员) 产品经理 市场专员(处方药)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
A. General Purpose and Scope:? Supervise study director and project management staff, responsible for the technical and scientificsupervision and conduct of Mammalian Toxicology studies. Responsible for the day to dayoperation and performance of the scientific staff within the Toxicology Study Direction andProject Management group. May maintain study director responsibilities for toxicology studies? Serves as a Project Manager and/or Study Director, as described in the GLPs. Has overallresponsibility for the client interactions, working with business development, projectmanagement including study designs for regulatory submissions, technical conduct of a studyas well as for the interpretation, analysis, documentation, and reporting of results? Managerial role for talent retention, career development, recruitment and employeeperformance evaluation? China Point of Contact in the global safety assessment working groups within CovanceB. Duties and Responsibilities:? Supervises the training of study directors/project managers and contributes to the training ofother staff members.? Oversees the scientific aspects of standard operating procedures, protocols and reports toensure full compliance with regulations.? Reviews and makes recommendations on research proposals for scientific feasibility and costbenefit perspectives.? Responsible for the development and implementation of plans, policies and procedures withindepartment guidelines to improve the work quality, efficiency and/or productivity of thesegroups.? Work closely with local and global teams as well as the leaders in other sites to ensure testingis completed by established deadlines in compliance with SOPs, GLPs and regulatory agencyguidelines.? Facilitates implementation of new technology to reduce errors and/or improve productivity andquality.Initiates, plans and implements staff development programs. Develops department capabilities and resources to meet both present and future needs.? Monitors progress toward meeting departmental goals and objectives, and takes required corrective action. Works with cross-site management to maintain harmonized processes, goals and objectives for Safety Assessment.? Provides technical or scientific expertise and guidance in study design and training.? Responsible for the corrective actions and issues resolution process for issues involving Toxicology Study Direction and Project Management.? Coordinates efforts of the study team? Develops protocols and ensures that the protocol, including any changes, is approved and is in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines.? Reviews cost estimates to ensure that all protocol/amendment driven work scope specifications have been included in the price estimation.? Understands financial status of ongoing studies.? Monitors progress and status of assigned studies. Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified.? Directs preparation of reports, ensures compliance with protocol and regulatory requirements, and submits them to the client.? Participates or hosts client visits and pre-study outline preparation.? Will serve as a mentor to newly hired Study Directors.? Capable to translate study protocols/reports between English and Chinese? Performs other related duties as assigned. 职能类别: 生物工程/生物制药
周浦康新公路3377号
Why Covance? At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We Offer Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. There is no better time to join us!
产品经理/高级产品经理 1-2万/月
计算机辅助新药设计研究员 0.8-1.7万/月
活性分析研究员/高级研究员 0.9-1.8万/月
临床应用经理(口腔) 6-8千/月
工程师 6-8千/月
SFE专员/主管 6-8千/月
回访专员 100元/天
分子生物学研究员(或助理研究员) 0.6-1.2万/月
粗纯技术员 4.5-7千/月
口服制剂助理研究员 4.2-7.5千/月
市场总监 1-1.5万/月
市场推广/策划 (职位编号:00747) 4.5-6千/月
医学联络专员 0.6-1.2万/月
细胞平台实验技术员 0.8-1万/月
上海相关职位: 医疗器械注册工程师 高级客户服务工程师 分析仪器销售经理-上海 Sr/CRA(高级)临床监查员(上海) 医药销售 大区经理 学术推广专员(处方药) 市场推广专员(会务专员) 产品经理 市场专员(处方药)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09