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艾昆纬医药科技(上海)有限公司

Operation Specialist【双休/五险一金,各种福利齐全。】

年底双薪
年底分红
带薪年假
五险一金
午餐补助
住房补助
节日礼物
技能培训

职位描述

Job Overview

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under guidance and support of senior operation team members.


Essential Functions

? To Prioritize and complete the assigned trainings on time.

? Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.

? To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming - Adverse Events(AE)/endpoint information

? determining initial/update status of incoming events

? database entry

? coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.

? Ensure to meet quality standards per project requirements.

? Ensure to meet productivity and delivery standards per project requirements.

? To ensure compliance to all project related processes and activities.

? Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.

? Creating, maintaining and tracking cases as applicable to the project plan.

? Identify quality problems, if any, and bring them to the attention of a senior team member.

? To demonstrate problem solving capabilities.

? Liaise with different functional team members, e.g. project management, clinical, data management

? health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.

? May liaise with client in relation to details on day to day case processing activities.

? To mentor new teams members, if assigned by the Manager.

? Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.

? Perform other duties as assigned.

? Lead/ Support department Initiatives

? 100% compliance towards all people practices and processes

? In addition to the above mentioned responsibilities, depending on the project requirement, the team member may perform medical review of non-serious adverse events (AEs) and non-serious adverse drug reactions (ADRs) which includes reviewal of AE coding, past medical history, concomitant medications, expectedness/ listedness, causality assessment and other medical information and ensure completeness and accuracy of data according to applicable regulations and guidelines, SOPs, project-specific guidelines, and medical evaluation guidelines and communicate with the team leads for any correction required in the case and maintain appropriate documentation for all communications.


Qualifications

? High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences Req

? Bachelor's degree in life sciences or related field and up to 3 years of relevant experience, inclusive of up to 1 year of Pharmacovigilance experience. Req

? or equivalent combination of education, training and experience. Pref

? Good knowledge of medical terminology. Intermediate

? Working knowledge of applicable Safety Database and any other internal/Client applications. Intermediate

? Knowledge of applicable global, regional, local clinical research regulatory requirements. Intermediate

? Excellent attention to detail and accuracy. Intermediate

? maintain high quality standards. Intermediate

? Good working knowledge of Microsoft Office and web-based applications. Intermediate

? Strong organizational skills and time management skills. Intermediate

? Strong verbal/written communication skills. Intermediate

? Self-motivated and flexible. Intermediate

? Ability to follow instructions/guidelines, utilize initiative and work independently. Intermediate

? Ability to multi-task, meet strict deadlines, manage competing priorities and changing demands. Intermediate

? Ability to delegate to less experienced team members. Intermediate

? Ability to be flexible and receptive to changing process demands. Intermediate

? Willingness and aptitude to learn new skills across Safety service lines. Intermediate

? Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Intermediate

? Ability to work as a Team Player, contribute and work towards achieving Team goals. Intermediate

? Ensure quality of deliverables according to the agreed terms. Intermediate

? Demonstration of IQVIA core values while doing daily tasks Advanced

? Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Intermediate

? Regular sitting for extended periods of time. Intermediate

? May require occasional tra

工作地点 大连市-高新区
薪资 9K-10K
语言 韩语/朝鲜语 英语/四级
学历 本科

艾昆纬医药科技(上海)有限公司

Operation Specialist 2【双休/五险一金,福利齐全。】

年底双薪
年底分红
带薪年假
五险一金
午餐补助
住房补助
节日礼物
技能培训

职位描述

Job Overview

Apply knowledge and expertise including complex decision making activities to review, assess and process Safety data and information across service lines. Recognized as specialist in one or more areas. Provide oversight on small to medium service operational projects and act as mentor to junior members of staff.


Essential Functions

? Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.

? To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information

? determining initial/update status of incoming events

? database entry

? coding AE and Products, writing narratives, Literature related activities, Quality review, assisting with reconciliation, case closure related activities, coordinating translations, as per internal/ project timelines. Creating, maintaining and tracking cases as applicable to the project plan.

? Perform activities related to adjudication as applicable

? Assess Safety data for reportability to relevant authorities, track reportable cases and report to regulatory authorities, ethics committees, institutional review boards, investigators, oversight groups per legislation, within timelines and in a format compatible to meet requirement as per project. Liaise with relevant stakeholders to facilitate expedited reporting.

? Liaise with manager for regulatory tracking requirements and electronic reporting.

? Contribute knowledge and expertise to or lead assigned deliverables in the field of Safety Publishing, Risk Management, Safety Surveillance and Medical Information or other service lines as appropriate.

? Ensure to meet quality, productivity and delivery standards per project requirements.

? Ensure compliance to all project related processes and activities.

? Build a positive, collaborative team environment with Safety team members, lead by example, provide training and mentoring for less experienced team members and operations staff, assist Operations Manager as a backup when needed.

? Provide and impart technical and process information to Safety Management and members of operational team on project specific issues.

? Provide oversight role and have a good understanding of operational team on status, metrics, productivity and initiatives.

? Maintain a thorough understanding of project protocol, therapeutic indication, budget and scope of work (SOW) for assigned projects

? set up and maintain project files, standard templates, electronic forms, databases and workflow as per project requirement.

? Establish and maintain effective team and project service operations communications i.e. provide regular feedback to operations team manager and other relevant stakeholders on project metrics, out of scope work challenges/issues and successes

? effective feedback on project performance to junior members of team.

? Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring completeness of individual training plan and maintain up to date training transcripts.

? Participate or Lead trainings across Safety process service offerings

? participate in working groups as applicable in implementation of new initiatives, identification and implementation of process efficiencies.

? To demonstrate problem solving capabilities.

? Liaise with different functional team members, e.g. project management, clinical, data management

? health care professionals e.g. investigators, medical monitors, site coordinators and designees to address project related issues.

? Attend project team meetings and provide regular feedback/ inputs to Operations team manager on operational project metrics, out of scope work challenges/issues and successes.

? To liaise with client in relation to details on day to day activities as needed.

? Contribute to achievement of departmental goals

? Perform other duties as assigned

? 100% compliance towards all people practices and processes

? In addition to the above mentioned responsibilities, depending on the project requirement, the team member may perform medical review of non-serious adverse events (AEs) and non-serious adverse drug reactions (ADRs) which includes reviewal of AE coding, past medical history, concomitant medications, expectedness/ listedness, causality assessment and other medical information and ensure completeness and accuracy of data according to applicable regulations and guidelines, SOPs, project-specific guidelines, and medical evaluation guidelines and communicate with the team leads for any correction required in the case and maintain appropriate documentation for all communications.


Qualifications

? Bachelor's Degree Scientific or healthcare discipline or allied life sciences Req

? Bachelor's degree in life sciences or related field and up to 5 years of relevant experience, inclusive of up to 3 years of Pharmacovigilance experience. Req

? or equivalent combination of education, training and experience. Pref

? Excellent knowledge of medical terminology. Intermediate

? In depth knowledge and understanding of applicable Safety Database and any other internal/Client applications. Advanced

? In depth knowledge and understanding of applicable global, regional, local clinical research regulatory requirements. Advanced

? Excellent organizational skills, time management skills, attention to detail and accuracy. Advanced

? maintain high quality standards. Advanced

? Excellent working knowledge of Microsoft Office and web-based applications. Intermediate

? To demonstrate effective project management and leadership skills. Intermediate

? Effective mentoring and coaching skills. Advanced

? Excellent verbal/written communication skills. Advanced

? Self-motivated, flexible, receptive to changing process demands. Advanced

? willingness and aptitude to learn new skills across Safety service lines. Advanced

? Proven ability to work independently and autonomously with policies and practices. Advanced

? Proven ability to multi-task, meet strict deadlines, manage competing priorities. Advanced

? Ability to identify, prioritize tasks and delegate to team members. Advanced

? Ability to establish and maintain effective communication and working relationships with coworkers, managers and clients. Advanced

? Ability to work as a Team Player, contribute and work towards achieving Team goals. Advanced

? Demonstrate Sound judgment and decision making skills. Advanced

? Ability to work effectively on multiple projects simultaneously, organize own workload and effectively manage teams’ priorities. Intermediate

? Ensure quality of deliverables according to the agreed terms. Advanced

? Demonstration of IQVIA core values while doing daily tasks. Advanced

? Skill to plan work load based on available capacity and ability to change prioritization based on workload fluctuations. Intermediate

? Skill to negotiate and work on finding a central ground that is satisfactory to all concerned stake holders. Intermediate

? Support audit preparedness Advanced

? Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Intermediate

? Regular sitting for extended periods of time. Intermediate

? May require occasional travel. Intermediate

? Flexibility to operate in shifts. Advanced

工作地点 大连市-高新区
薪资 14K-16K
语言 韩语/朝鲜语 英语/四级
学历 本科

深圳市蓝禾技术有限公司

日本内容营销【体系完善、团队氛围、五险一金+双休】

年底双薪
绩效奖金
年底分红
带薪年假
交通补助
五险一金
午餐补助
住房补助
节日礼物
技能培训

职位描述

岗位职责:1.创意策划与内容生产:

基于项目,结合产品卖点,营销策略和品牌定位,生产出适用于红人推广、广告投放、品牌宣传事件的内容,达成品宣目标(如推广Brief、视频脚本、品牌文案等)。

2.渠道推广内容数据分析:

能主动收集、整理和分析内容生产相关的各渠道数据,从内容和转化率角度分析数据结果,为渠道、内容提出改进和优化建议。

3.追踪趋势性热点内容并复制传播:

针对海外热点进行捕捉,有内容复制能力,能够捕捉到热点进行内容二创和传播。

4.渠道内容共创:

能与渠道合作方一起沟通协作,进行品牌、营销内容共创。


任职要求:

1.本科及以上学历,市场营销、商务管理等相关专业优先,有内容策划,短视频制作相关经验优先,具备良好的日语听说读写能力。

2.熟悉海外媒体生态环境,具备良好的沟通、谈判和协商能力,具备团队合作精神。

3.熟悉行业市场和竞争情况,具备市场调研和分析能力。

4.对于海外热点有敏锐度,喜欢冲浪海外社交媒体。


工作地点 深圳市-龙华新区
薪资 9K-12K
语言 日语/N1
学历 本科
职位描述

◆总公司地址:兵库县神户市

◆成   立:1951年

◆资本金:201亿6700万日元

◆年销售额:1838亿5900万日元

◆员工数:8706名(截止2022年末)


◆岗位:营业企划职

◆人数:1名

◆年龄:25~40岁

◆工作地:兵库县明石市(总部工厂)

◆国籍:不限

◆学历:本科及以上

◆语音能力:日语日常会话

◆必要证书:驾照(赴日后可更换成日本驾照)

◆经验年数:3年及以上工作经验,有营业企画或者海外业务开拓经验

◆计算机:PC技能


◆必要能力:中文、英语、日语能力(以上语言能力均需至少流利沟通),策划能力及策划书制作能力


◆业务内容:

■本期招聘目标是培养将来的海外市场负责人。与海外现地集团公司及日本国内开发部门协作,根据当地的市场调查,进行商品开发(包括制作企划书),除了该业务之外,还将参与集团公司的业绩管理。

■本公司在海外17个国家有业务发展。

【业务场景:(例)中国市场】

■中国由于经济增长,不仅是上海、北京等一二线城市,三四线城市对热水器等产品的需求也在增加,今后市场会继续扩大。国内外已有很多竞争企业,本公司也致力于对中国事业部进行组改,集中力量扩宽中国市场。


◆要求:

■有制作企划书、推动项目经验的人

■懂英语、中文及日语的人

■学习积极性高,愿意且有能力持续学习的人


◆其他特别事项

【欢迎】

■有制造业工作经验的人

◎当地法人中也有日本员工,交流基本上以日语为主。

◎将来可能会调到全球总部内的北美事业部、亚洲大洋洲事业部(工作地不变),根据情况也有可能到海外赴任。


◆月薪:33.5万日元~

※根据实际成绩、经验、奖金、津贴有变动

◆全年奖金:年2次(4.37个月工资)

 ※根据2023年度成绩、业绩

◆年总收入:550-700万日元

◆加班补贴:有

◆交通补贴:有

◆住宅补贴:有

◆餐费补贴:员工食堂有折扣

◆其他补贴:参照福利说明

◆涨薪:每年1次(4月)

◆试用期间:3个月(待遇基本不变)

◆工资结算日:20号

◆工资支付日:月末

◆工作日:周一至周五

◆休息日:每周2天

◆工作时间:8:50~17:50    工作8小时,休息时间1小时

◆加班:有

◆每月平均加班时间:20小时

◆带薪休假:全年休息日125天、年末年初、GW、夏季休假、リフレッシュ休假(连续工作10年、20年、30年)等

◆社会保险:社会保险完善


◆福利:

Benefit station(各种员工打折服务)健康保险组合、厚生年金基金、企业退休金制度、確定拠出年金制度、財形貯蓄、员工持股会、团体保险等。

全公司共同教育(新员工研修、新人跟进研修、晋升必须研修等)、指定研修(职业研修等)、选择式自我启发教育(能力开发研讨会、公共资格取得支援、通信教育等)、部门教育(营业职研修、研究开发职研修等)。


◆入社研修:根据各部门要求(导入研修、OJT等)

◆公司住宅:有

◆其他:企业有员工宿舍,房租为员工自己承担;如有需要人才也可以提出自己的要求,企业可以根据人才要求寻找合适的住房,有住房补贴。

工作地点 关西兵库县
薪资 15K-20K
语言 日语/N1 英语/四级
学历 本科

深圳市德科信息技术有限公司

游戏运营【带薪年假、交通补助、午餐补助、节日礼物、六险一金、弹性工作 】

年底双薪
带薪年假
交通补助
午餐补助
节日礼物
管理规范
六险一金
弹性工作

职位描述

岗位职责:
1. 参与/负责游戏运营支持开发跟进和营销活动的设计开发跟进。
2. 参与/负责游戏在海外市场的本地化工作。
3. 负责游戏玩家相关的社区营造和维护。

岗位要求:
1. 具备熟练的英语/日语听说读写能力,对海外用户有深入的理解。
2. 具有海外项目的研发与运营经验,有卡牌类游戏经验优先。
3. 善于沟通,有团队合作精神,对待工作有责任心。
4. 热爱游戏,能承受一定强度的工作压力。

工作地点 广州市-天河区
薪资 6K-12K
语言 日语/N1
学历 本科
职位描述

数字营销销售(日籍or中国籍日语人才)


【日籍】年轻人选、有广告Or互联网相关经验即可、国内 在日都可

【中国籍日语人才】日语商务水平,行业经验要求较高


【薪资基本】15k左右  提成另算

【福利】五险一金  补充医疗  团建  节日福利 年假10天+ 

【关键词】TOB销售相关经验  沟通能力好social能力强  互联网广告营销  数字营销  


【岗位职责】

(1)负责面向广告主/广告代理公司销售公司互联网广告产品和服务,执行并完成公司销售指标及收款;

(2)根据销售任务,制定中、短期销售计划,并定期汇报;

(3)开发、维护新老客户的合作关系,并保持业绩稳定增长;

(4)准确理解客户的网络广告需求,回复客户查询并推荐媒体、演示、面对面销售、报价、谈判、签约等

(5)与相关部门协作,向客户提供专业而全面的售前、售中及售后服务,保证客户需求顺利实现。


【任职要求】

(1)从事互联网广告销售3年以上经验,熟悉互联网广告市场;

(2)优秀的沟通能力和销售技巧,能够独立地和广告客户沟通,能独立定制客户方案,积极寻求让客户满意的策略,有成功管理客户的经验;

(3)工作主动性强,有创业精神,有较强的创新能力;

(4)销售管理经验优先;

(5)会日语或英语更佳。

工作地点 上海市-黄浦区
薪资 15K-18K
语言 日语/N1
学历 本科
职位描述

一、岗位职责:

1.营运资金报告编制;

2.投资管理;

3.经营数据汇总情,协助预测利润、分析损益;

4.韩语翻译。


二、任职要求:

1.全日制本科及以上学历,经管、财会类相关专业;

2.熟练使用电脑及办公软件Excel、Word、PPT;

3.工作认真细致,责任心强,诚实可靠;

4.较敏捷的思维,创新求变的意识;

5.有较强的沟通能力、组织协调能力;

6.韩语优秀者优先考虑;

工作地点 广州市-黄埔区
薪资 6K-7K
语言 韩语/朝鲜语
学历 本科

北京夜神数娱科技有限公司

英语海外运营【双休/五险一金,欧美海外出差。】

年底双薪
专项奖金
绩效奖金
带薪年假
五险一金
定期体检
年度旅游
节日礼物
管理规范
技能培训
岗位晋升

职位描述

【工作内容】

1. 负责全线移动端产品的海外用户获取工作。

2. 从数据出发,以用户增长为工作目标,制定推广策略,不断探索新的用户获取方法。

3. 关注行业增长策略,综合运用各类方法达成增长目标。


【工作要去】

1、1年以上海外用户运营经验,欧美地区优先。

2、英语熟练,可作为工作语言,有留学经历优先。

3、掌握各类海外推广渠道和用户增长方法优先;

4、有较强的推广活动执行能力优先。

5、具备优秀的自我驱动力,数据敏感度,执行力。

工作地点 北京市-海淀区
薪资 10K-18K
语言 英语/六级
学历 本科

北京夜神数娱科技有限公司

印尼语运营【双休/五险一金,年底双薪,带薪年假。】

年底双薪
专项奖金
绩效奖金
带薪年假
五险一金
定期体检
年度旅游
节日礼物
管理规范
技能培训
岗位晋升

职位描述

【工作内容】

1. 负责夜神系列产品在海外地区的推广运营,包括新渠道开拓,内容、用户、活动的日常运营,拉高海外用户活跃度,进行流量变现,塑造品牌效应。

2. 作为国际版产品的用户反馈接口,基于用户反馈不断提出产品优化建议,促进产品持续迭代。

3. 监控海外竞品动态,对运营数据进行分析并调整运营策略,根据分析进行用户调研。


【工作要求】

1. 本科及以上学历,有海外运营推广工作经验,有印尼语方向工作经验者优先。

2. 较强的沟通能力、合作意识、推动力、执行力,学习能力。

工作地点 北京市-海淀区
薪资 8K-15K
语言 马来语
学历 本科

北京夜神数娱科技有限公司

泰语运营【年底双薪,带薪年假,发展空间大。】

年底双薪
专项奖金
绩效奖金
带薪年假
五险一金
定期体检
年度旅游
节日礼物
管理规范
技能培训
岗位晋升

职位描述

【工作内容】

1.  负责夜神系列产品在海外地区的推广运营,包括新渠道开拓,内容、用户、活动的日常运营,拉高海外用户活跃度,进行流量变现,塑造品牌效应。

2.  监控海外竞品动态,对运营数据进行分析并调整运营策略,根据分析进行用户调研和输出建议报告。


【工作要求】

1.  本科及泰语专业学生,爱好海外运营推广工作。

2.  较强的沟通能力、合作意识、推动力、执行力,学习能力。

3.  英语书面表达能力强,口语、书写流利;

4.  同时欢迎优秀在校生、应届生。

工作地点 北京市-海淀区
薪资 6K-10K
语言 泰语 英语/未应试
学历 本科
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