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无工作经验 -
招1人 -
11-09 发布
- 五险一金
- 绩效奖金
- 节日福利
- 住房补贴
- 体检
职位描述
职位描述： 工作职责?Support the tasks below for assigned project throughout the study:oResponsible for Trial Master File (TMF)/PTMF maintenance in accordance with ICH-GCP and SOPs (ELARA scanning, indexing and QC within prescribed timelines)oUpdates the trial and site information as necessary in Corporate Clinical Trial Registry (CCTR) in a timely mannero Attends appropriate training programs and project teleconferences as applicable.oMaintains the study status tracking and provides analysis report to Study Manager.oAassits Study Manager on study budget control by timely tracking and reporting of actual cost and forecast drafting.oCoordinates Clinical Study Agreement approval to ensure site initiation on time.?Study Start-UpoSupports and coordinates the clinical trial application to ethics committee and regulatory authority, if applicable, to obtain approval within required timeline.oCoordinates and applies for export/import license of, lab kits, equipments, and specimen, if applicable.oAssists on the preparation, compilation, accuracy review and correction of Investigator Initiation Package (IIP) documents and obtaining approval(s) to ensure drug release in the defined timelines.oSupports for preparation of site initiation packages (e.g. SMF)oOrganizes investigator meeting in country/regional baseoAssists Study Manager on PTMF SSDL setup through communication with global study owner as necessary.?Study ConductoSupports and coordinates the clinical trial application for amendment and progress report to ethics committee and regulatory authority, if applicable, and obtain approval within required timeline.oEnsures along with the CRA the reconciliation of Trial Master File and the Site Master File on a periodic basis.oMaintains / develops local tracking spreadsheets for study-related documents, data, tasks and activities, as applicable.oAssists CRA for the responsibility of tracking, distribution and filing of clinical trial documents/information (e.g. paper CRFs, DCFs ) with quality review for accuracy and completeness.?Study Close-OutoEnsures along with the CRA the reconciliation of Trial Master File and the Site Master FileoSupports SM and CRA for final archive of study-related documentsoEnsures study payment completion.Other responsibilities of the CTA:oSupports CQL for quality improve related initiativesoAssists in preparation of newsletters and other study-related documents.oComplies with Pfizer Policies, SOPs & IGs and local regulations during various projects related transactionsoTakes SME role and provides training to CRA / SM regularly.oEnsures P2L and GCOLT Metrics Compliance pertaining to CTA role.oProvides back-up coverage for other CTAs as necessary.oMentors new CTA when applicable (apply for B4 level)oSupports CTA Lead for production and tracking of trial metrics measurements.oSupports SM for coordinating with sites for finalizing budget worksheets and contractual agreements (e.g. FCPA clauses).oMaintains and ensures the availability of inventory for all non drug supplies.oProvides logistic and administrative support to project teams.oAssists on SUSAR package preparation for Ethics Committee and regulatory authority, if applicableoDemonstrates and promotes Pfizer global value system across all interactions.任职资格?College degree or above?Good English skills in writing and reading?Proficiency in basic computer literacy (e.g. Microsoft word, Excel and PowerPoint)?3 years of clinical research experience(apply for B4 level)?Knowledge of ICH GCP and local regulations?Experience in management of clinical trial and/or regulatory documents?Knowledge of application used in the clinical trials 职能类别： 临床研究员
联系方式
北京
公司信息
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，是目前全球最大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“ ”。我们的使命是“ ”。 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.
