专业要求：
学历要求：本科及以上
工作经验：不限
薪资待遇：面议
招聘人数：1
招聘对象： 社会人才
1. 本科或以上学历，市场营销、广告、传播等相关专业优先。
2. 具有英文听说读写能力，CET6（或同等）以上，有海外留学背景优先。
3. 熟悉影视娱乐产业，尤其对电影产业有浓厚兴趣。
4. 相关活动公司／公关公司策划执行或实习经验至少1年。
5. 积极的工作态度，对工作充满热忱，热爱学习。
6. 出色的管理、协调及组织能力。
7. 熟练操作相关办公软件，会做美美的PPT/Keynote、会简单PS者优先。
工作职责：
1. 能主动为活动设计提供想法和建议，并整合成方案。
2. 协助负责活动概念规划，活动创意设计对接。
3. 协助活动的实施和管理，按照时间规划积极跟进提案内容。
4. 管理并维护良好的内外部资源。
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工作地区： 北京 学历要求：本科及以上性别要求：不限
工作经验：不限薪资待遇：8001-10000 月薪招聘人数： 1
公司性质：私营企业公司规模：1 - 49人所属行业：IC其他企业
职位描述：
Job Purpose ·Prepares (from technical perspective) documents for further processing, review, expediting to be performed by CPO DS&E/PVO.·Ensure technical compliance of documents with technical guidelines·Support the DS&E/PVO team in their document management duties e.g., formatting documents, QC of documents, archiving·To support management of DS&E/PVO operational processes at Country Pharma Organization (CPO) in ensuring compliance with Client company global/local procedures, national and international regulations/ standards/guidelines for pharmacovigilance of Client company marketed and investigational productsMajor Accountabilities 1.Prepares the respective submission documents to Health Authorities2.Supervision of proper flow of confirmations of receipt of documentation sent to the Health Authorities.3.Preparation and everyday distribution of respective DS&E documents externally.4.Participation in the verification process of data correctness in the global safety database.5.Verification of correctness and compliance of documentation sent to CPO DS&E Department:·Internal documents translation·Verification if a document sent to DS&E grant the safety requirements of the internal materials as described in respective Client company procedures6.Preparation of the CPO DS&E training materials (incl. confirmations) and logistic organization of these trainings·Editing (where required and as per request from CPO DS&E Member) training materials·Preparation of confirmations, certificates, printing of training materials for participants7.Archiving all safety documentation as per respective policies, guidance and procedures.8.Verification and update of respective CPO DS&E archiving system (incl. review, update, management)9.Manage collection, processing, documentation, reporting and follow-up of all serious adverse events (SAE) reports for all Client company products from clinical trials, post-marketing studies (PMS), registries, and all adverse events from commercial, sales and marketing programs and all Spontaneous Reports (SR).10.Transcribe, translate and enter data of all Serious Adverse Events (from Clinical Trials, post-marketing studies (PMS), registries) and all adverse events (from commercial, sales and marketing programs and all Spontaneous Reports) from source documents onto safety systems (e.g. Argus Affiliate, etc) accurately and consistently with emphasis on timeliness and quality.11.Record and track receipts, submissions and distributions of SAEs, SRs, Investigator Notifications (IN)/Suspected Unexpected Serious Adverse Reaction (SUSAR), Periodic Safety Report Updates (PSUR) and Development Safety Update Report (DSUR).12.Manage reporting/submission/distribution of safety reports/updates/information (e.g. SAE, SR, IN, PSUR, Biannual SUSAR Listing, DSUR) to Local Health Authorities (LHA) and/or clinical operations.13.Work with other local/global PVO associates to ensure accurate evaluation of safety data.14.Interact and exchange relevant safety information with LHA, PVO associates, other functional groups and third party contractor, if applicable.15.Support in developing, updating and implementing local procedures to ensure compliance with PVO global procedures and national requirements.16.Input, review and approval of program proposals for language, content and establishment of necessary controls on collection and reporting of adverse event information.17.Perform reconciliation with other departments (e.g. Medical Information, Quality Assurance and third party contractor, if applicable) for potential AEs resulting from medical inquiries and quality related complaints.Key Performance Indicators ·Completeness and correctness of the data received and sent out in respective tracking tools/systems·Timely preparation of dispatch·Timely introduction of the respective data into the system/tracking tool·Timely and quality of prepared documentation, training materials·Completeness, clarity and compliance of the archived DS&E documentation with global and local Client company standards·CPO AE reporting compliance·Results of audits/inspections·Customer feedback
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