Project Planner - FSP
1-1.3万·13薪
 上海-浦东新区
 1-3年
 本科
 全职
 更新于03-30
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职位信息

"Planning/Controlling (Scheduling and Resource Management)
61 Responsible for coordinating, monitoring and reporting project schedule and resource management information to enable alignment of PRD and partner line schedules and FTE/dollar resources. These schedules include:
o Clinical study plans (Protocol Development to Final Clinical Study Report) and Clinical Operation Submission activities to support Module 1 and 5 of the submission plan.
61 Identifies and raises schedule conflicts, risks, and resource peaks/troughs appropriately for resolution.
61 Directly participates in and contributes to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.
61 Monitors progress of project activities towards next project milestone, anticipates and highlights potential variances, supports line/team in critical path analyses and understanding the impact.
61 Performs scenario planning of project timelines within and across protocols and across disease area/portfolio to enable optimum use of local, global, and outsourced resources to ensure efficient delivery of project milestones.
Project Execution and Delivery
61 Partners with key team members (e.g., PM, Medicinal Sciences, CS&O, DSRD, Commercial) to manage the project and achieve key milestones according to the endorsed timeline, cost, and quality parameters.
61 Contributes to risk management through the identification of operational and project/program risks for discussion with appropriate team leadership. Participates in team discussions to de-risk projects and develop new options to resolve moderately complex issues.
61 Provides the Portfolio Management group with project schedule information to enable effective portfolio management activities.
Analysis and Reporting
61 Produces what-if scenario analyses (base, optimistic and pessimistic development) based on context obtained from project team members (e.g. PM, Medicinal Sciences, CS&O, DSRD, Commercial). Decisions taken by the team based on these analyses may impact project delivery, costs, and resource requirements.
61 Reviews own work regarding quality of schedule and resource metadata through utilization of quality reports and monitoring/management of such data with the team/line members.
61 Provides timely reporting to the PM, Portfolio Management, and project teams, alerting them to the possibility of endangered/missed or conflicting milestones and critical path activities.
61 Ensures regular information updates and analysis and interpretation of planning and forecasting data to project teams, Portfolio Management, platform lines, and management teams.
61 Utilizes available reporting and visualization tools to support governance and team reporting needs (e.g. OnePager, Business Objects, Spotfire).
61 Provides context to local customers of reports generated globally and consolidates customer feedback to enable improvement of existing reports and generation of new reports.
Process
61 Partners with project team members (e.g. PM, Medicinal Sciences, CS&O, DSRD, Commercial) to identify opportunities and potential solutions to realize efficiency in the development process.
61 Contributes to continuous improvement of project plans, plan generation, plan utilization, and/or report creation/development processes.
"
"Education
61 Bachelors level degree.
61 B.S. with 2+ years' experience or M.S. with 1-2 years' experience.
Experience
61 At least 1 year experience in project planning and project management.
61 At least 2 years’ experience in pharmaceutical industry or related/similar industry.
Beneficial Relevant Capabilities
61 Project Management Professional (PMP) certification preferred but not required.
61 Experienced in end-game/regulatory submission planning and/or product launch planning.
61 Experienced with planning and resource forecasting tools (e.g., MS Project, Planisware, OnePager).
61 Experienced user of reporting and office software (e.g., MS Office, Business Objects, Spotfire).
61 Trained/experienced in negotiation, facilitation and managing cross-functional team dynamics."
工作地址
 东亚银行金融大厦
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公司信息
精鼎医药(Parexel International)是全球领先的药物研究合同委托机构(CRO),总部位于美国生物医药圣地马萨诸塞州的波士顿附近,在世界各地拥有71个办事处,约17,600 名员工,为超过100个国家的客户提供服务。
精鼎医药成立于1982年,在三十多年的历程中,一直致力于发展成为全球生物制药和医疗器械行业首屈一指的新型医学疗法开发和商业化服务供应商,并且取得了卓越成果。目前,我们能够提供全世界CRO领域全面的新药临床阶段研发服务,服务内容包括新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床试验数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、临床试验供应和物流服务、临床电子数据采集、临床医学信息管理系统、新药查验登记事务和国际临床试验相关法规咨询等。
将我们的全球法规监管专业经验、I-IV期临床研究服务、整合的电子化临床技术能力和商业化服务结合在一起的一体化解决方案,可帮助我们的客户更加顺畅、经济和高效的推动整个研发历程。
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img精鼎医药研究开发(上海)有限公司
外资(欧美)
10000人以上
制药/生物工程
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