邢台招聘

Role Description
(Items identified with subscript(ADM02) are required by ADM-02. Any updates to this role description should include updating the date field in the footer.)

Position Title(ADM02):Data & Document Processing Associate
Reports To(ADM02):Team Lead of Data & Document Processing Associates
Assignment Duration(ADM02): Contracted resource
Zone / Line:Clinical Data Services (CDS), Pfizer Wuhan R&D Center (WRDC)
Career Ladder (Level):D1-3

Position Purpose(ADM02):
The Data & Document Processing Associate (DDPA) is responsible for providing accurate and efficient support for the data process of projects and document process tasks that are assigned to the Wuhan office. The DDPA enters and verifies clinical data into corresponding clinical trial databases from images or electric file (i.e. case report forms, laboratory reports, translation data list), performs data entry QC, resolves E-task, cleans index review queries, setup eclipse study specific structure and other data and document processes as instructed. The DDPA for clinical trials works closely with Clinical Data Management in CDS and may assist with other document handling and administrative tasks as necessary.

Organizational Relationships(ADM02):
Reports to team lead – Data and Document Processing

Key Result Areas (ADM02):
Data and Document process:
· Enter Clinical Data into Clinical Database with minimal errors based on quality standards and maintains an acceptable level of productivity to assist in meeting project deadlines.
· Perform data entry (1st & 2nd pass), including corrections to ensure that data entered into database accurately reflects the data recorded on the CRF or according to project guidelines as assigned.
· Fulfills requirements for tracking or documenting work processed.
· Perform QC in accordance with data entry guidelines and other project specific documents by comparing data listings to the data source (CRFs/hard copy documentation/scanned images) to establish accuracy rate.
· Resolve e-task and clean up Index Review queue on a daily basis.
· Communicate with Data Managers of all Pfizer Studies via e-mail and GCDStrack tickets to clarify standard eclipse process or execution of their request.
· Setup eclipse study specific structure and perform QC in accordance with ESS worksheet and give feed back to SSU with timelines for business continuity.
· Provide PGRD/PGP Submission Compilation Group with Case record documentation within given timelines.
· Ensure documents are properly labelled by drug, protocol, investigator, and subject, and that site personnel are aware of the requirements for submitting documents to Development Operations.
· Perform QC in CRT (Casebook Review Tool) & CXT (Casebook Exraction Tool ) in accordance with submission assembly guideline.
· Participates in the manual review of clinical data and identification and documentation of data errors, omissions and inconsistencies.
· Coordinates destruction of outdated, unnecessary confidential internal CDM and study specific documentation and prepares data for archiving.
· Follow instruction on document process and complete assignment in a timely matter.
· Performs other clinical trial data and document processing tasks as necessary to meet the needs of business.

General
· Perform data entry and other computer work for extended periods of time as the primary function of the position.
· Proactively seek to improve the efficiency and quality of work.
Liaise regularly with supervisor to assess workload and priority activities and status of assigned tasks and projects.

Personal Development
· Attend and actively participate in personal development courses as required. Attend Pfizer in house training and workshops.
· Develop skills and experiences for broader role responsibilities in the data and document processing area such as working knowledge of database, electronic document management systemand other Data Processing tools and develop experience in second entry verification, quality control and/ or manual processes.
· Assist documentation tracking, project management, or solve issues and suggest solutions.
· Develop technical expertise and project management skills.

Education & Experience Preferred(ADM02):
Education:
· College graduates with good English skill both in writing and speaking.

Experience:
· Knowledge of Windows Environment and its applications, keyboard skills.
· Familiarity with medical terminology; Prior clinical data entry experience is preferred.

Competencies 技能要求(ADM02):
· Capability to communicate effectively in English, both verbally and written is required.
· Must be accurate and have an excellent attention to detail and a methodical approach to work.
· Must have a basic concept of the importance of data quality control.
· Must have ability to work on multiple projects with different processing guidelines.
· Demonstrated organizational skills.
· Must enjoy working with computers and technology.
· Must enjoy working with people and be interested in good customer service.

Desirable Requirement:
· Proficiency at typing or previous clinical data entry experience.
· Computer literate and the ability to understand and carry out detailed instructions.
· Medical environment work experience.

简历收集邮箱：job-c2.china@pfizer.com

辉瑞公司（Pfizer Inc.）创建于1849年，迄今已有160多年的历史，总部位于美国纽约，是目前全球***的以研发为基础的生物制药公司。辉瑞致力于运用创新的科学技术以及全球资源来改善每个生命阶段的健康和福祉。
我们的目标是“不断创新为患者带来能显著改善其健康的药物”。我们的使命是“成为一家卓越的创新型生物制药公司”。
2012年辉瑞公司全年合计收入590亿美元，研发投入78亿美元。辉瑞在全球拥有9万多名员工，59家生产基地，业务遍及全球150多个国家和地区。2012年财富全球500强企业中辉瑞排名126位。
目前辉瑞公司的产品覆盖了包括化学药物、生物制剂、疫苗、健康药物、动物保健品等用于人类、动物和消费者保健等诸多广泛而极具潜力的治疗及健康领域，同时其卓越的研发和生产能力处于全球领先地位。
在人类和动物药品的发现、开发和生产过程中，辉瑞始终致力于奉行严格的质量、安全和价值标准。每天，分布在世界各地的辉瑞员工致力于促进当地医疗卫生的发展以及探索能够应对当今最为棘手疾病的预防和治疗方案。
辉瑞还与世界各地的医疗卫生专业人士、政府和社区合作，支持世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家世界领先的生物制药公司的责任是一致的。160多年来，辉瑞一直努力为人们提供更好、更优质的服务。
辉瑞生物制药目前在华上市的创新药物已超过50个，其治疗领域涵盖了心脑血管及代谢、抗感染、中枢神经、抗炎镇痛、抗肿瘤、泌尿、疫苗及等诸多领域。其中如立普妥®、络活喜®、万艾可®、舒普深®、希舒美®、沛儿®、索坦®许多产品在市场上处于领先地位。为了让中国的广大患者能及时接受与全球同步的先进的药物治疗，辉瑞未来将进一步加大和加快在华新药引进和上市的力度和速度。
辉瑞健康药物旗下的善存®、钙尔奇®、惠菲宁®等消费保健产品也在中国市场家喻户晓，并以其优异的品质深受广大消费者的青睐；辉瑞旗下的硕腾动物保健品*为中国的动物保健市场提供各类领先的动物疫苗和动物药品。

At Pfizer, we apply science and our global resources to improve health and well-being at every stage of life. We strive to set the standard for quality, safety and value in the discovery, development and manufacturing of medicines for people and animals. Our diversified global health care portfolio includes human and animal biologic and small molecule medicines and vaccines, as well as nutritional products of healthcare industry and many of the world's best-known healthcare products such as Centrum. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as the world's leading biopharmaceutical company, we also collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 160 years, Pfizer has worked to make a difference for all who rely on us.