-
无工作经验 -
硕士 -
招2人 -
12-01 发布
- 五险一金
- 专业培训
- 出国机会
- 年终奖金
- 弹性工作
职位描述
职位描述： Responsibilities1)Coordinating internal resources and third parties/vendors for the flawless execution of clinical trial projects according to GCP quality standards2)Ensuring that all projects are delivered on-time, within scope and within budget3)Ensuring resource availability and allocationJob BriefWe are looking for an experienced Project Manager with proven experience in managing phase I to Phase III clinical trials according to GCP quality standardsto manage organization of key pharmaceutical development projects.Job DutiesProject management responsibilities include delivering every project on time within budget and scope. Project manager should have an education or working background track record in biotechnology or pharmaceutical fields, and experiences in management, budgeting and analysis.Project manager shall be skilled at getting the best out of the people and projects that he/she oversees, shall thrive when planning projects and working with project associated CRO and/or CMO teams.The detailed responsibilities include:1)Managing contract research organizations, which are involved in the clinical trial execution2)Management of and collaboration with clinical trial investigators and study nurses3)Responsibility for clinical trial site establishment and management4)Responsibility for online and clinical trial site quality control of Clinical Research Files (CRF’s)5)Coordinate of internal resources and third parties/vendors for the flawless execution of projects;6)Responsibility for clinical trial material handling and clinical site shipments7)Responsibility for clinical trial quality control8)Responsibility for clinical trial database management9)Ensure that all projects are delivered on-time, within scope and within budget;10)Developing project scopes and objectives, involving all relevant stakeholders and ensuring technical feasibility;11)Ensure resource availability and allocation;12)Develop a detailed project plan to track progress;13)Use appropriate verification techniques to manage changes in project scope, schedule and costs;14)Measure project performance using appropriate systems, tools and techniques;15)Report regularly and escalate to senior management level as needed;16)Manage the relationship with the associated collaborators and all stakeholders;17)Perform risk management to minimize project risks;18)Establish and maintain relationships with third parties/vendors;19)Create and maintain comprehensive project documentation.Requirements1)Proven GCP training skills2)Great educational background, preferably in the fields of biotechnology science or engineering, pharmaceutical, or medical science;3)Proven working experience as a project administrator in the biotechnology or pharmaceutical sector;4)Solid technical background, with understanding or hands-on experience in pharmaceutical development and relevant technologies;5)Excellent external and internal communication skills and good team player;6)Excellent written and verbal communication skills, preferably in both English and Chinese;7)Solid organizational skills including attention to detail and multi-tasking skills;8)Strong working knowledge of Microsoft Office and online clinical trial management software;9)Oversea education/working experience, or working experience in international companies is a plus 职能类别： 医药技术研发管理人员 项目管理
联系方式
苏州工业园区纳米城西北区11幢204室
公司信息
R & D, sales: Bio pharmaceutical, cosmetics, reagents and supplies, laboratory equipment, medical equipment, camera equipment, computer software and hardware, and provide related technical consulting, technology services, technology transfer, technical support, in the above products and technology import and export business.
