- 目录
岗位职责是什么
数据经理是一个关键角色，负责组织的数据战略、管理和分析，以支持业务决策和推动企业增长。此职位的核心在于将数据转化为可操作的洞察，为企业提供竞争优势。
岗位职责要求
1. 具备深厚的统计学和数据分析知识，熟悉sql、python、r等数据处理工具。
2. 精通数据可视化工具，如tableau或power bi，能创建清晰、有影响力的报告。
3. 熟悉数据库管理，包括数据清洗、整合和存储。
4. 强烈的商业意识，理解业务需求并能将其转化为数据驱动的解决方案。
5. 出色的沟通技巧，能向非技术人员解释复杂的分析结果。
6. 领导能力，能够指导和管理数据团队，确保项目按时完成。
7. 对数据隐私和合规性有深入的理解，遵守相关法规。
岗位职责描述
数据经理在日常工作中，负责规划和执行数据收集策略，确保数据质量和准确性。他们需要挖掘大数据，识别模式和趋势，为管理层提供战略建议。此外，他们还需与其他部门合作，将数据洞察融入产品开发、市场营销和运营决策中。数据经理还必须监督数据安全，防止数据泄露，并确保符合gdpr等数据保护法规。
有哪些内容
1. 数据战略制定：定义数据管理的目标和流程，确保数据资产的有效利用。
2. 团队管理：招聘、培训和管理数据团队，提升团队效率和专业技能。
3. 数据分析与报告：进行复杂的数据分析，生成易于理解的报告，揭示业务机会和挑战。
4. 业务合作：与各部门合作，提供数据支持，解答业务问题，优化业务流程。
5. 系统维护与升级：评估和实施新的数据工具和技术，优化数据基础设施。
6. 数据质量保证：监控数据质量，实施数据清洗和校正流程，确保数据的准确性和完整性。
7. 合规性管理：确保所有数据操作符合行业标准和法律法规，维护企业声誉。
数据经理的角色是多面的，既需要技术专长，又需要商业洞察力，他们在企业的数字化转型中扮演着至关重要的角色，通过数据驱动的决策，帮助企业实现持续的业务增长和创新。
数据经理岗位职责范文
第1篇 数据经理岗位职责
大数据副总经理 赣州市国有资产投资集团有限公司 赣州市国有资产投资集团有限公司 岗位职责:
全面负责大数据中心的技术战略规划和企业管理工作
岗位要求:
1.国家211工程全日制研究生及以上学历,具有硕士及以上学位,年龄在45周岁(1973年11月1日以后出生)以内,中共党员优先;
2.10年及以上计算机及互联网公司、咨询公司等大型企业战略规划、企业管理等相关工作经验,熟悉政府行业和互联网行业;
3.具有多个大型系统集成项目管理经验,单个项目合同规模不低于5千万;
4.具备前瞻性思维、优秀的市场分析能力与市场洞察预测能力;
5.热爱并善于研究新知识,具有优秀的学习能力;
6.具有优秀的职业素养,具有强烈的事业心,团队协作意识强,工作责任心强;
7.具有项目管理中高级职称者优先。
第2篇 临床数据经理岗位职责
临床数据经理 primary activities include, but are not limited to:
? all responsibilities of a clinical data manager.
? assume data management responsibilities for larger, more comple_ or higher priority protocols.
? may coordinate general ad-hoc sponsor data entry (sde) process for the protocol, discuss timelines, and provide data entry status to the clinical development scientist (cds).
? provide protocol specific training of sde process to cdm.
? triage, research, discuss and resolve the reports outputs provided by clinical development scientist (cds) and statisticians at a protocol level during in-life and database lock stages supported by the lcdm.
? supports the lcdm in the preparation, creation and review of data management tool specifications and tools
? participates in user acceptance testing (uat) of the clinical database repository under the direction of the lcdm.
? coordinates communications, global status tracking and issue resolution at study level with lead cdm (lcdm).
? responsible for the communication with clinical trial operations team regarding site level issues on protocol a basis on behalf of the lcdm.
? monitor protocol level cycle time performance (metrics) and follow up on specific countries/sites metrics issues and deliver status and resolution updates to lcdm.
? responsible for study level status assessment, reporting and communication with lcdm.
? complete trial level archiving activities under the direction of the lcdm including, but not limited to, filing of essential documentation.
? coordinate and mentor cdms and other scdms who work in his/ her protocol to ensure their compliance with sops, data management plans and data review plans.
? be assigned to special responsibilities related to process maintenance, data quality assessment, staff training and mentoring and/ or other special activities, such as providing inputs to create or update sops, supporting documents and training materials as needed.
? may be required to support dmc process owner (po) models in the local dmc and/or in the global po networks.
? participate in cross functional technical or process improvement projects.
manual encoding lead
? perform all responsibilities of a manual encoder under the clinical data manager.
? ensure encoding accuracy and consistency across all protocols within a project.
? works closely with dmc manual encoders and data management trial manager (dmtm) to ensure all encoding tasks are completed prior to interim analysis, frozen files/ database locks.
? serves as subject matter e_pert (sme) for encoding documents and processes.
? responsible to review specified therapeutic area encoding as requested.
? coordinates with lcdm to create and review encoding specifications documents and performs user acceptance testing (uat) of coding application (s).
? responsible for encoding e_ternal partner data as applicable and consultant for contract research organization (cro) partners.
? runs encoding check reports in accordance with data review plans to identify encoding issues.
? raises questions with investigational site staff or dmc manual encoders and reviews responses and corresponding data corrections to confirm resolution.
? responsible for study level encoding status reporting and assessment, and communication with dmc clinical trial (ct) management during in-life data management activities and preparation for database lock.
requirements
education:
1. at least b.a. or b.s. degree, preferably in medicine, pharmacy, nursing, biological sciences, or health care related discipline.
knowledge and skills:
1. two years’ e_perience in clinical data management in pharmaceutical or health care clinical research environment is preferable.
2. self-motivated, e_cellent in work planning and time management.
3. fluent oral and written english skills.
4. good basic awareness of the clinical development process.
5. good basic awareness of clinical practice and grasp of medical terminology.
6. good sense and awareness of regulations and policies.
7. able to work under pressure and in a changing environment with fle_ibility.
8. good communication skills with the ability to communicate with both technical and business areas.
9. proven leadership skills, specifically the ability to coordinate the work of others and influence management on decision making. primary activities include, but are not limited to:
? all responsibilities of a clinical data manager.
? assume data management responsibilities for larger, more comple_ or higher priority protocols.
? may coordinate general ad-hoc sponsor data entry (sde) process for the protocol, discuss timelines, and provide data entry status to the clinical development scientist (cds).
? provide protocol specific training of sde process to cdm.
? triage, research, discuss and resolve the reports outputs provided by clinical development scientist (cds) and statisticians at a protocol level during in-life and database lock stages supported by the lcdm.
? supports the lcdm in the preparation, creation and review of data management tool specifications and tools
? participates in user acceptance testing (uat) of the clinical database repository under the direction of the lcdm.
? coordinates communications, global status tracking and issue resolution at study level with lead cdm (lcdm).
? responsible for the communication with clinical trial operations team regarding site level issues on protocol a basis on behalf of the lcdm.
? monitor protocol level cycle time performance (metrics) and follow up on specific countries/sites metrics issues and deliver status and resolution updates to lcdm.
? responsible for study level status assessment, reporting and communication with lcdm.
? complete trial level archiving activities under the direction of the lcdm including, but not limited to, filing of essential documentation.
? coordinate and mentor cdms and other scdms who work in his/ her protocol to ensure their compliance with sops, data management plans and data review plans.
? be assigned to special responsibilities related to process maintenance, data quality assessment, staff training and mentoring and/ or other special activities, such as providing inputs to create or update sops, supporting documents and training materials as needed.
? may be required to support dmc process owner (po) models in the local dmc and/or in the global po networks.
? participate in cross functional technical or process improvement projects.
manual encoding lead
? perform all responsibilities of a manual encoder under the clinical data manager.
? ensure encoding accuracy and consistency across all protocols within a project.
? works closely with dmc manual encoders and data management trial manager (dmtm) to ensure all encoding tasks are completed prior to interim analysis, frozen files/ database locks.
? serves as subject matter e_pert (sme) for encoding documents and processes.
? responsible to review specified therapeutic area encoding as requested.
? coordinates with lcdm to create and review encoding specifications documents and performs user acceptance testing (uat) of coding application (s).
? responsible for encoding e_ternal partner data as applicable and consultant for contract research organization (cro) partners.
? runs encoding check reports in accordance with data review plans to identify encoding issues.
? raises questions with investigational site staff or dmc manual encoders and reviews responses and corresponding data corrections to confirm resolution.
? responsible for study level encoding status reporting and assessment, and communication with dmc clinical trial (ct) management during in-life data management activities and preparation for database lock.
requirements
education:
1. at least b.a. or b.s. degree, preferably in medicine, pharmacy, nursing, biological sciences, or health care related discipline.
knowledge and skills:
1. two years’ e_perience in clinical data management in pharmaceutical or health care clinical research environment is preferable.
2. self-motivated, e_cellent in work planning and time management.
3. fluent oral and written english skills.
4. good basic awareness of the clinical development process.
5. good basic awareness of clinical practice and grasp of medical terminology.
6. good sense and awareness of regulations and policies.
7. able to work under pressure and in a changing environment with fle_ibility.
8. good communication skills with the ability to communicate with both technical and business areas.
9. proven leadership skills, specifically the ability to coordinate the work of others and influence management on decision making.
