长沙招聘

工作职责:

Line:Global Product Development (GPD) / Clinical Sciences & Operations / Development China/ Portfolio & Project Management/ Project Planning

Location:Shanghai

Role Summary:The Supervisor, Project Planner applies skills and general drug development knowledge to contribute to the achievement of team goals and is responsible for the generation, management, and maintenance of high quality project schedules associated with the drug development teams supporting the operational/strategic delivery of new medicines to patients.  He/she may support several different types of schedules in support of a clinical development plan, which may include but are not limited to: medicine, clinical studies.  The Supervisor, Project Planner possesses a general knowledge/understanding of drug development, associated business processes, and project planning software and plays a key role in scenario planning, i.e., building schedule options.

任职资格:

Organizational Relationships:Reports directly to Manager/Sr Manager Project Planner.  Works under general supervision and typically receives guidance on more complex problems and scenarios.  The Supervisor, Project Planner works primarily in a cross-functional or matrixed team environment and is expected to ensure his/her work meets expected standards, but work may require review by team members or leadership.

Partners primarily with Clinical Project Managers (CPMs), Asset Planner and members of project teams, protocol teams, and partner lines (e.g. Medicinal Sciences, Clinical Sciences and Operations

CS&O

, Drug Safety Research & Development

DSRD

, Commercial) to ensure accurate, integrated project planning at the medicine and study level.

Resources Managed (budget and FTEs):This role does not have budgetary responsibility or direct reports.

Responsibilities:Responsible for performing important project planning activities in support of team deliverables and the GPD portfolio.  To effectively execute the primary responsibilities, the Supervisor, Project Planner may work within a cross-functional team environment supporting moderately complex projects but may also assist a more senior Project Planner or CPM in support of more complex project deliverables.  The colleague partners with the CPM and team members in support of Development, Operations, and Commercial project team members and partner line representatives to create project schedules that enable effective planning and ensure project delivery.  The colleague must possess knowledge of the principles and concepts of project management.  The colleague is expected to apply technical and team knowledge along with scheduling knowledge to contribute to the achievement of team and GPD deliverables.

Planning/Controlling (Scheduling and Resource Management)

Responsible for coordinating, monitoring and reporting project schedule information to enable alignment of GPD and partner line schedules. These schedules include: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.

Identifies and raises schedule conflicts, risks appropriately for resolution.

Directly participates in and contributes to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules.

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.

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

Partners with key team members (e.g., PPM, Medicinal Sciences, CS&O, DSRD, Commercial) to manage the project and achieve key milestones according to the endorsed timeline, cost, and quality parameters.

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.

Provides the Portfolio Management group with project schedule information to enable effective portfolio management activities.

Analysis and Reporting

Produces what-if scenario analyses (base, optimistic and pessimistic development) based on context obtained from project team members (e.g. PPM, Medicinal Sciences, CS&O, DSRD, Commercial).  Decisions taken by the team based on these analyses may impact project delivery, costs, and resource requirements.

Reviews own work regarding quality of schedule through utilization of quality reports and monitoring/management of such data with the team/line members.

Provides timely reporting to the PM, Portfolio Management, and project teams, "alert"ing them to the possibility of endangered/missed or conflicting milestones and critical path activities.

Ensures regular information updates and analysis and interpretation of planning and forecasting data to project teams, Portfolio Management, platform lines, and management teams.

Utilizes available reporting and visualization tools to support governance and team reporting needs (e.g. OnePager, Business Objects, Spotfire).

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

Partners with project team members (e.g. PPM, Medicinal Sciences, CS&O, DSRD, Commercial) to identify opportunities and potential solutions to realize efficiency in the development process.

Contributes to continuous improvement of project plans, plan generation, plan utilization, and/or report creation/development processes.

Collaborates with colleagues to ensure cross-team, site learnings, and best practices are shared.

Promotes partner lines/teams taking ownership of data within planning tools to help them manage their business.

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards.
辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。