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临床研究采购经理(J23000)

面议

北京市本科及以上7年及以上

发布时间:2023-09-06

职位描述

工作职责:
JOB SUMMARY
Working collaboratively across the Medicinal Sciences organization, the Clinical Research Sourcing Strategist (CRSS) develops cost effective, flexible commercial product sourcing strategies for the lifecycle of clinical development programs.
In this role, your experiences will enable you to work both internally and externally to oversee and manage operational aspects of supply chain projects. Your experience in project management will enable transparent delivery of projects and budgets, that meet productivity, quality, and customer-satisfaction goals.
While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks, recommend next practices for improvements and influence teams to achieve targets.
任职资格:
JOB RESPONSIBILITIES
You will be the Global Clinical Supply (GCS) point of contact to develop sourcing strategies for commercial products in clinical development programs.
You will participate on GCS and cross-organizational study teams to understand clinical trial protocol design and determine commercial product supply needs.
You will collaborate internally with Clinical Supply Strategy and Management (CSSM), Drug Product Supply (DPS), Global Product Development (GPD) and Clinical Research Pharmacy (CRP) teams, and externally with suppliers, to develop creative commercial product sourcing options across central, local, site and specialty sourcing options.
You will be responsible for selecting the appropriate vendor from an established vendor pool by assessing total cost, timelines, risk, and supply chain complexity.
You will consider supplier capabilities including product access, inventory management, label assessment, depot management and distribution.
You will develop and communicate the optimal sourcing strategy to your internal customer(s) and ensure continuity of commercial product supply for the duration of the protocol.
You will participate in vendor meetings and utilize available business tools to ensure project success.
You will work with partner lines and the vendor to manage purchase orders and invoicing, operational timelines and regulatory and quality compliance throughout the lifecycle of the protocol.
You will maintain compliance to the CRSS training curriculum, providing feedback on procedural and process improvements to reflect a CRSS end to end sourcing strategy model.
BASIC QUALIFICATIONS
Training & Education:
Must-Have
B.A or B.S. degree is required.
2~3 yrs of professional experience within global clinical supply in a pharmaceutical company or relevant industry experience.
Customer oriented with the ability to work across multiple teams to influence strategic decisions that will provide cost saving to projects.
Proven ability to effectively develop, communicate, and gain support for execution of plans with a wide range of stakeholders.
Collaborations within multi-disciplinary teams that includes innovating, measuring work, negotiation, straight talk and delivering to milestones.
Ability to manage a large budget and associated financial aspects to deliver on time against tight timelines.
Experience managing change in a dynamic, complex environment.
Demonstrated interest in Patient Quality and Compliance.
Nice-to-Have
Training in project management, supply chain management, scientific or clinical disciplines, business administration and/or people development.
Experience with drug development, clinical study design, scientific research, and / or pharmaceutical manufacturing.
Experience with strategic sourcing, packaging, labeling and distribution and supplier management are highly desirable.
Background or experience in clinical site operations and clinical trial execution with medical or drug market knowledge would be advantageo**************************

其他要求

  • 1人
  • 临床研究经理CRM

公司介绍

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。

辉瑞(中国)研究开发有限公司

行业:
制药.生物
规模:
1-49人
性质:
其他
地址:
1(邮编:200000)

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