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临床受试者招募专员西斯比亚(北京)医药技术研究有限责任公司北京0.6-1万/月10-15

学历要求:大专|工作经验:1年|公司性质:外资(欧美)|公司规模:150-500人

Responsibilities for Patient Recruitment SpecialistTo obtain thorough knowledge of the clinical trial protocols.To obtain thorough knowledge of the CCBR controlled documents and procedures.To have thorough knowledge of ICH GCP and any relevant national and international law and regulation for performing clinical trials.To obtain thorough knowledge of and understanding about recruiting subjects for clinical trials.To develop new Health Centers and Communities relationships for patient recruitment.To establish and maintain relationship with Health Centers and Communities.To serve as a liaison between the company and Health Centers and Communities.Tasks for Patient Recruitment SpecialistTo meet patient recruitment targets of different trails.To identify and resolve concerns from Health Centers and Communities.To develop and implement plans of patient recruitments.To review patient recruitment materials.To emphasize on the importance of communications among all parties during a studyrecruitment period.To maximize recruiting efforts in a cost effective manner.To establish subject target groups for the clinical trialsTo complete ad hoc projects assigned by Manag

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临床研究助理 CTA北京翰兰德医药科技发展有限公司武汉5-8千/月10-15

学历要求:本科|工作经验:1年|公司性质:民营公司|公司规模:少于50人

根据GCP和研究方案要求,协助监查员完成临床试验的监查工作。协助监查员完成对于项目进度和质量的跟进协调项目管理会议,会议后的跟进,会议记录撰写协助监查员完成研究资料的收集、归档和管理工作... 任职要求 临床医学、护理、药学等相关专业毕业,在医院有工作经验者(医疗护理或临床研究)优先具有踏实、敬业的工作态度,良好的人际关良好的沟通和协调能力熟练使用办公常用软件,包括word, excel, powerpoint等强的独立工作能力及团队合作精神 良好的身体素质,能适应高强度工作,适应短期出差

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Junior Application Engineer 应用工程师麦朗(上海)医疗器材贸易有限公司武汉-江汉区6-8千/月10-15

学历要求:本科|工作经验:1年|公司性质:外资(欧美)|公司规模:150-500人

Responsibilities for this position include:Willing to follow/support/collaborate with team to complete research or assignment with direction by supervisor.Inspections, scientific analysis and testing to address chemistry-related issues related to the use of materials in applications to medical devicesExtensive search of journals, articles, patents, new innovative technologies, products etc. for the new product development in the Medical Device field.Assignments will require the ability to gather information from and convey technical conclusions to individuals in engineering, business, law and industry.A significant portion of activities will include root cause analysis of a wide variety of failures related to issues arising in development, manufacturing or use of products manufactured for the medical device industries. Qualifications for this position include:Bachelors in Non-woven, Polymer/Materials Science, Chemical engineering or a related major; Master degree preferred2021 fresh graduatesExcellent written and oral EnglishStrong communication skillStrong teamwork Project experience is a plusKnowledge of product/manufacture related is a plus.

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临床技术支持(武汉)(J10330)先健科技(深圳)有限公司武汉1-1.5万/月10-15

学历要求:本科|工作经验:2年|公司性质:外资(非欧美)|公司规模:500-1000人

工作职责:1.协助临床医师使用公司相关产品完成手术,并协助解决术者在使用相关产品时遇到的问题2.协助医生完成产品相关的学术文献及幻灯片的编写3.负责临床医师的产品使用培训4.负责内部员工产品知识培训5.收集产品在临床中使用反馈6.协助研发部门评估在研产品的临床效果7.协助销售团队处理产品使用过程中遇到的技术问题8.协助销售团队维护大客户并开发有潜力客户任职资格:1. 本科以上学历,生物医药类相关专业,临床医学专业尤佳;2. 两年以上医疗器械行业临床技术支持相关经验或具有临床医生工作经历;3. 具有心内科、心外科临床工作经历者优先;4. 具有良好的沟通能力和学习能力,适应出差。

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验收员湖北人福医药集团有限公司武汉-东湖新技术产业开发区3.5-5千/月10-14

学历要求:大专|工作经验:1年|公司性质:民营公司|公司规模:150-500人

岗位职责:1、负责到货药品质量验收;按照《药品验收操作规程》、《医疗器械验收操作规程》按比例进行抽样验收,检查到货产品外观质量。根据验收情况,将验收结论、产品批号、效期、生产日期信息录入到WMS系统。2、负责有效期较近、破损污染等质量异常情况的上报;3、负责药品入库情况的详细记录,对未入库品种、药品需及时跟踪入库情况,并了解未入库原因;4、负责入库单据的打印及保管。任职资格:1、医学检验专业或中药学专业,具有检验师初级或中药学初级以上专业技术职称优先考虑;2、熟悉GSP验收工作流程,具有良好的沟通能力,1年以上同等岗位工作经验优先;3、具备药品、器械产品基础知识,熟练办公软件,以及其它需要更新的知识。4、工作细致认真,责任心强,思维敏捷,肯吃苦耐劳,具有较强的团队合作精神。

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中药资源劲牌有限公司黄石0.8-1万/月10-01

学历要求:本科|工作经验:3-4年|公司性质:民营公司|公司规模:10000人以上

1、负责中药材资源产地信息及市场行情的分析工作; 2、负责中药材产地供应商开发工作;3、负责保健酒和配方颗粒中药材产地考察及评价工作; 4、负责制定保健酒和配方颗粒中药材质量验收标准及其修订工作;5、负责配方颗粒药材回货质量验收工作。任职要求:1、熟悉中药资源研究的方法和思路;2、熟悉HPLC、TLC、IR-UV等实验分析仪器操作;3、熟悉中药鉴定学、中药化学、植物分类学、中药资源学、中药栽培学、生药学相关知识;4、熟悉保健食品与中医药相关研发流程;5、熟悉中药材种植技术。

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项目/课题研究助理广州白云山中一药业有限公司武汉-蔡甸区4.5-6千/月09-15

学历要求:本科|工作经验:无需经验|公司性质:国企|公司规模:1000-5000人

工作职责:1.协助课题组成员进行卵巢早衰的基础及相关转化实验操作及研究;2.协助样本库管理。岗位要求:要求:1.分子生物学、生物化学、药理学、医学、细胞生物学、临床医学或中药学专业本科或以上学历;2.能够独立开展动物实验,熟练掌握细胞培养、皮下肿瘤接种、腹腔动脉采血和眼眶取血、病理切片、常规病理染色、ELISA试剂盒检测、PCR、westernblot等实验技术,具有卵巢早衰课题研究经验者优先考虑;3.具有良好的英语写作能力;4.诚实守信、敬业忠诚、有奉献精神、责任心强、对科学研究有热情、注重团队合作精神,并恪守科研道德;5.根据公司需要,同意配合公司外派到外省合作单位(拟定为武汉中国健康谷附近)进行2年科研工作。备注:该岗位为项目科研助理,为劳务派遣性质。项目结束后,工作表现优异者可转正。

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医学联络官 MSL默沙东(中国)投资有限公司湖北省09-10

学历要求:本科|工作经验:2年|公司性质:外资(欧美)|公司规模:

OVERALL JOB PURPOSE AND PRIMARY ACTIVITIES·        Medical Science Liaisons are field-based medical professional serves as an advocate for MSD science within the healthcare community. ·        Medical Scientific Liaisons are scientifically trained and credentialed therapeutic area, disease, and product experts who engage in non-promotional scientific exchange with SLs or KDMs (Scientific Leaders or Key Decision Makers). MSLs develop and execute on action plans aligned with the Guiding Principles for Ex-US GMA External Stakeholder-Facing Activities, local and global company policies, local rules & regulations, and the Medical Affairs Plan (MAP).·        The MSL is responsible for ensuring that he/she is fully versed in the therapeutic area and up-to-date on all major studies, both ongoing and completed, product information on Merck’s and other companies’ relevant therapies, clinical data and relevant pipeline data to provide the most balanced data to SLs, KDMS and the healthcare community to improve patient care.·        The MSL is a field-based medical professional whose primary responsibility is to engage in non-promotional peer-to-peer communication & provide medical/scientific information to SLs and KDMs based on cutting-edge scientific exchange and services oriented towards the stakeholder’s professional interests & needs.MAIN RESPONSIBILITIESEngagement with External ExpertsEngaging in non-promotional peer-to-peer exchange of medical and scientific information with SLs or KDMs to the extent permitted by law and local regulation, local industry codes, and other provisions of the Guiding Principles for Ex-US GMA External Stakeholder-Facing Activities.Gaining deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in their local geography.Representing Medical Affairs at local or regional non-promotional Medical events (e.g. Medical Congresses and Symposia). They may collaborate in the coordination of pre-event scientific information and post-event scientific summaries.Responding to unsolicited requests for medical, scientific, pipeline or marketed product information or indications from SLs or KDMs utilizing appropriate approved scientific materials.Responding (one-to-one) to unsolicited requests for information on company research and/or grant activities by directing SLs or KDMs to appropriate company resources for grants, sponsored clinical trial involvement, Merck Investigator Study Program (MISP), and outcomes research.Organizing and participating in medical and scientific exchange activities, which include but not limited in hospital lecture, journal club, experts input forum, advisory boards, may take the role as presenter.On a reactive basis, can share the publically available AOIs with SLs and direct them to the website for further information.Providing medical/scientific support, including written documentation and/or verbal interactions for Health Technology Assessments (HTA) and formulary decisions. Such support is provided following the principles of scientific exchange as outlined in the Guiding Principles for Ex-US GMA External Stakeholder-Facing Activities.Internal SupportFormulating regional Medical Affairs Plans (rMAP) and implementation of activities identified in the rMAP.At Global Clinical Trials Organization (GCTO), GDSA, or Center for Observational and Real World Research (CORE) personnel request, supporting the identification of potential study investigators for sponsored study.Providing insights internally on the scientific gaps, ideas and other topics gathered from scientific exchange to inform MISP Areas of Interest, development programs, and company TA strategy.Supporting company commercial colleagues by providing on-label or disease state scientific training to MSD personnel in the therapeutic area when requested and where allowed.Provide scientific support to patient access program.   EducationAdvanced scientific degree is strongly preferred, such as MD (or equivalent MB.Ch.B.), PharmD, or PhD in a life science, preferably with clinical knowledge of assigned therapeutic area. At minimum, college education degree in pharmacy.Experience·        Minimum of 2 years of pharmaceutical experience is strongly preferred. Experience in assigned therapeutic area is highly preferred.   ·        Strong scientific baseline knowledge in assigned therapeutic area(s), clinical trial methods, implementation and data interpretation, sound scientific and clinical judgment, and eagerness to continue to learn more in depth about a specific therapeutic area·        Ability to present scientific and other technical information with confidence, in a way that engenders trust and credibility.·        Excellent communication skills across a variety of internal and external audiences including listening skills and probing skills.·        Strong collaboration skills and ability to function within a team environment.·        Ability to handle multiple tasks at the same time and work under pressure.·        Fluent English, fluent office software technology.·        Be able to travel at least monthly

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诊断试剂研发工程师(J17456)深圳华大基因股份有限公司武汉1-1.5万/月08-23

学历要求:硕士|工作经验:3-4年|公司性质:上市公司|公司规模:1000-5000人

工作职责:1、负责体外诊断试剂产品开发,设计实验、建立和优化反应体系、评估产品性能;2、负责研发过程中实验结果的记录、分析、汇报;3、制定产品工艺方案,编制工艺文件;4、参与产品生产转化,解决产品生产过程中的相关问题;5、撰写技术报告及专利文件,参与注册资料准备,配合完成产品注册申报;6、上级交办的其他工作。任职资格:1、 生物学、分子生物学、微生物学等相关专业,硕士及以上学历;2、 熟练掌握核酸提取、荧光定量PCR、序列分析及引物探针设计等分子生物学技术;3、 或熟练掌握免疫诊断相关技术,具有免疫诊断试剂研发经验;4、 具有2年以上相关工作经验,能够独立开发体外诊断试剂产品;5、 有良好的英文文献阅读能力和文字表达能力,有较强的实验操作能力、分析能力和问题解决能力;6、 具有优秀的执行力和团队精神。

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Sterilization Intern灭菌实习生麦朗(上海)医疗器材贸易有限公司武汉-江汉区120元/天10-15

学历要求:本科|工作经验:在校生/应届生|公司性质:外资(欧美)|公司规模:150-500人

Responsibilities:·  Agreement update ·  Sterilization related data summarize and analysis ·  Review calibration certificates ·  Document uploads ·  Other routine supports assigned by supervisor ·  Internal communication with team membersRequirement:·  Bachelor degree, major in science or engineering is preferred; ·  Strong English writing skill; ·  Strong communication skill ·  Responsible ·  Positive work attitude

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仓库管理员-包住宿湖北人福医药集团有限公司武汉-东湖新技术产业开发区2-4千/月10-14

学历要求:大专|工作经验:在校生/应届生|公司性质:民营公司|公司规模:150-500人

1、负责药品进出仓库管理,保证出入库药品质量完好,数量准确无误;2、负责药品库存管理,药品堆放有序,定期盘点库存情况,并做报告分析;3、负责拒收、缺货、销售退回、购进退出等各项记录,并及时向上级领导反馈;4、负责根据客户单位要货计划,对发货药品进行分类配送;5、仓库的规范管理,仓库日常盘点、清洁、归纳、整理等。任职要求:1、药学等相关专业,有库管工作经验优先;2、熟悉GSP保管工作流程,具有良好的沟通能力;3、工作细致认真,责任心强,思维敏捷,具有较强的团队合作精神。工作地点:湖北省武汉市东湖新技术开发区神墩二路96号

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