临床检验技术岗位职责

临床检验技术岗位职责共3篇(医学检验岗位职责要求)

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　　下面是范文网小编分享的临床检验技术岗位职责共3篇(医学检验岗位职责要求)，供大家赏析。

临床检验技术岗位职责共1

　　委托临床检验招标技术要求

　　乙方（投标医疗机构）须向甲方（XX医院）提供如下文件，加盖公章，协议进行期间提供的文件有变更时，应提前或在变更后一周内重新提交，并保持所提供的文件现行有效；其中的人员资质、受委托项目质量文件、投标检验项目优惠收费价格及技术能力等文件可在中标后签署合同时补齐。

　　一、投标单位提供基本资质

　　1、机构资质及服务项目

　　（1）医疗机构及年度校验合格资质；

　　（2）临床基因扩增检验实验室资质及其它卫生行政主管部门要求具备的资质；

　　（3）实验室质量管理体系认可、认证或权威评审的证明材料；

　　（4）检验项目表，收费标准及其在《XX统一医疗服务收费标准》上的编码。

　　2、人员资质

　　（1）实验室质量负责人、技术负责人卫生技术专业资格证书；

　　（2）受委托检验项目检验操作、报告签字人员卫生技术专业资格证书；

　　3、受委托检验项目质量文件

　　（1）受委托实验室质量文件目录：如程序文件、作业指导书、质量记录；

　　（2）受委托检验室检验服务流程方案；

　　（3）受委托检验项目检验申请、样本采集、样本保存与运输的程序要求；

　　（4）受委托检验项目结果结果报告、咨询、投诉程序与声明；

　　（5）受委托检验项目的室间质评证书；

　　（6）受委托检验项目典型检验报告样单；

　　（7）受托实验室再次委托其它实验室检测时，参照上述要求提交文件材料。

　　二、投标检验项目优惠收费价格及技术能力

　　根据下列外送检验项目需求，填写投标检验项目收费技术能力表，乙方如非北京市基本医疗保险定点医疗机构，需向甲方提交将甲方医保标本委托给具备医保定点医疗机构资检验的保证书。

　　肺炎支原体抗体(IgM) 肺炎支原体抗体(IgG) 肺炎衣原体抗体(IgM) 肺炎衣原体抗体(IgG) EB病毒抗体IgM EB病毒抗体IgG EB病毒抗体IgA EB病毒全套检测 单纯疱疹Ⅰ病毒(IgM) 单纯疱疹Ⅰ病毒(IgG) 单纯疱疹Ⅱ病毒(IgM) 单纯疱疹Ⅱ病毒(IgG) 风疹病毒(IgM) 风疹病毒(IgG) 弓形体抗体(IgM) 弓形体抗体(IgG) 巨细胞病毒(IgM) 巨细胞病毒(IgG) 柯萨奇病毒抗体(IgM) 柯萨奇病毒抗体(IgG) 军团菌 丙肝病毒RNA测定 冷凝集 肥达反应外裴氏反应抗心磷脂抗体 促肾上腺皮质激素（ACTH）皮质醇生长激素 肾素-血管紧张素-醛固酮（立位）肾素-血管紧张素-醛固酮（卧位）儿茶酚胺 肝纤四项 胰岛细胞抗体（ICA） 胰岛素自身抗体（IAA）谷氨酸脱羧酶抗体(GAD) 胰高血糖素 降钙素 血药浓度（环孢A） 血药浓度（卡马西平）血药浓度（氨茶碱）血药浓度（苯妥英钠）血药浓度（丙戊酸）白介素10 肿瘤坏死因子 EPO浓度 G试验、GM试验 CD

　　55、CD59 免疫分型（骨髓、外周血）染色体（骨髓、外周血）AL32种融合基因筛查 CML或ALL BCR-ABL组合筛查 JAK2 V617和exon12基因突变筛查等。

　　临床检验室岗位职责

　　临床检验体液组岗位职责

　　临床高级专业技术岗位职责

　　临床检验士岗位职责（共11篇）

　　临床检验岗位职责年度总结

临床检验技术岗位职责共2

　　临床检验医师职责

　　1.根据临床信息，对检验项目的选择、检验申请、患者准备以及样品的采集、运送、保存、处理、检测和结果给予指导、培训、答疑和咨询。

　　2.参与临床查房和疑难、危重病例的会诊,对检验结果做出解释,并依据实验室结果对临床诊断和治疗提出建议。

　　3.负责签发具有诊断性的临床检验报告。

　　4.掌握检验项目的临床意义及临床医师的需要和要求,用循证医学的方法评价检验项目,制订疾病诊断指标的合理组合,规划和开展临床检验的新项目,并推动其临床应用。

　　5.高效率地收集和评估临床医护人员对检验工作效率和质量的反馈意见,组织持续改进。

　　6.指导和培训临床医护人员和实验室技术人员,提高教育质量,推动教学改革。

　　7.承担与实验室诊断相关的科研任务。

临床检验技术岗位职责共3

　　实验动物饲养与技术人员

　　实验动物饲养管理人员协助研究人员做饲养管理和一些基本的实验操作。协同其他员工例如兽医的工作人员，技术研究人员和部门经理等。

　　岗位职责：

　　日常实验动物的健康检查，喂水喂料，笼具更换清洗等 动物设施设备的清洁卫生 动物的接收运送 正确记录日常活动

　　工作中符合实验动物相关法规

　　协同其他员工的工作例如实验技术人员和部门经理等进行相关的实验

　　任职要求：

　　动物相关学科专科以上，考虑到工作性质和一定体力要求，优先考虑男性 读懂英文操作规范，英文好的优先 有实验动物抓取保定经验的优先考虑 能吃苦耐劳，身体健康

　　Animal Care Technician Animal Care Technicians are needed to aist research personnel by performing routine care and handling of laboratory animals and basic research Care Technicians will interact with a variety of positions including supervisors/managers, veterinarians, technicians and research personnel.

　　Responsibilities will include Daily health checks, feeding, watering, changing/cleaning cages for rodents, rabbits, dogs and primates Sanitize equipment and facilities Receive animal shipments and house animals appropriately Document work accurately Comply with all animal handling and animal welfare regulations and with regulatory

　　Qualifications and Experience Qualifications and Experience

　　Certificate of college biology technology or animal science Some animal handling experience Ability to follow written procedures Some lifting required

　　临床病理（检验）实验室技术人员

　　岗位职责：

　　临床病理实验室主要从事GLP实验中血液、尿液及骨髓标本的检验及分析。

　　岗位要求：

　　1.临床检验专业本科或兽医学、兽医病理学、兽医病理学与病理生理学硕士； 2.有临床检验实验室工作经验优先； 3.熟练操作计算机能力

　　4.良好的英语交流及读写能力；

　　5.优秀的团队精神、工作踏实，具有较强事业心。

　　Clinical Pathology Technician – Beijing, PRC The Clinical Pathology Tech provides services to animal toxicology studies by examining and analyzing biological fluids in support of preclinical research and development /she is responsible for aisting in all aspects of clinical pathology and be supervised by the head of clinical pathology to proce specimens for clinical pathology evaluation.

　　Responsibilities will include: Operate the instruments including Advia 2120 hematology system, clinitek Atlas automated urine chemistry analyzer, Hitachi 7080 serum chemistry analyzer and ACL 9000 coagulation system and relevant instruments to analyze the blood smear and bone marrow smear and have ability in methanol fixative and Wright-Giemsa in reports on serum chemistry, coagulation, urinalysis and hematology legible permanent record of all results obtained together with supporting all job aignments are performed in compliance with GLP and Experience MS in biological science or Clinical pathology related field BS in animal pathology is preferred in pharmaceutical industry and GLP requirements and written communications skills in handling biological samples

　　生物分析技术员 I

　　生物分析技术员I，将在FDA的相关指导下进行临床前期的生物分析和制剂分析研究中样品的提取和分析仪器的维护。生物分析技术员I 应遵循GLP规定，进行规范的数据记录的实验文件保存。该职位向药代动力技术主管汇报。

　　职位描述：

　　1.制剂分析（稳定性、均一性和浓度验证）；

　　2.样品的提取，例如在生物体液和组织中，用蛋白沉淀法、液液萃取、和固相萃取法提取生物样品；

　　3.负责分析仪器的操作、维护和故障维修； 4.遵守所有相关GLP的要求；

　　5.能够独立工作并具有团队合作精神，有良好的人际沟通技巧。

　　任职要求：

　　1.应具有药代动力学，药学、分析化学或相关领域的大专或本科学位； 2.

　　在生物样品（血浆、组织等）提取方面有0-5年的工作经验。

　　Aociate I, Analysis and Bioanalysis – Beijing, PRC

　　The Aociate I, Analysis and Bioanalysis, will aist in sample proceing per FDA guidance, implementing and maintaining analytical and bioanalytical aays and automated systems to support preclinical analytical and bioanalytical Aociate I, Analysis and Bioanalysis, must maintain GLP compliance in supporting preclinical studies and accurately document all Aociate I, Analysis and Bioanalysis, will report to the DMPK Technical will include:

　　1.

　　Conduct dose formulation analysis (stability, homogeneity and

　　concentration verification).2.

　　Conduct sample preparation and extraction such as protein precipitation,

　　liquid-liquid extraction and solid-phase extraction in biological fluids and

　　Take the responsibility for operation, maintenance and trouble-shooting of analytical

　　Comply with all applicable GLP

　　Work either individually or in an interdisciplinary team and poe excellent communication and interpersonal : 1.

　　 或Junior college in the pharmacokinetic analysis, pharmaceutical sciences, analytical chemistry or related fields 2.

　　With 0-5 years of experiences of sample proceing for biological samples (plasma, tiues, etc)

　　配药制剂技术员I Aociate Formulation

　　主要职责描述：

　　进行日常性口服和灌胃用药化合物的制剂的准备和配制，以支持对生物体内的药物代谢动力学，毒物学和药理学的相关实验； 执行英文实验数据记录和操作步骤的撰写； 在团队中进行有效的内部协作和沟通；

　　支持供试药品的管理和保证配药流程符合GLP要求。

　　任职要求：

　　应聘者应具有药学，药剂学或者或分析化学大专或本科学位； 具有小分子和大分子（蛋白或多肽）制剂配制者优先考虑； 有相关GLP经验和知识背景的优先；

　　良好的英语书写和口语沟通能力及熟练的计算机操作能力。

　　Main Responsibility Description Conduct routine formulation preparations and developments for oral and parenteral dosage forms to support in vivo pharmacokinetics, toxicology and pharmacology data record and formulation procedure in English.

　　Effectively interact and communicate within a dynamic team test article logistic and formulation procedures in GLP practice the ideal candidate should poe at least college diploma in pharmaceutical sciences/pharmacy/analytical chemistry with 0-5 years of experience.

　　Experience with formulation preparation both for small molecules and protein/peptides are highly ability to work independently and in a team environment, and excellent written and verbal communication and good computer skills are candidate with a good understanding about GLP regulations is of pharmacokinetics and drug metabolism in drug research and development are desirable, but not required.

　　Aociate I, Pharmacology The Aociate I Pharmacology will collect, document, and manage pertinent data including animal observations, test material administration, clinical sample collection, animal surgery and measurement of ECG, respiratory function and CNS FOB and test, etc in compliance with appropriate SOPs, or she will aist the study director in the conduct of pharmacology and safety pharmacology studies.

　　Responsibilities will include:

　　1.

　　Comprehend and follow study protocols and SOPs for GLP / Non-GLP

　　Comply with GLP documentation requirements, including data recording, reviewing and

　　Animal handling, observation, dosing, blood withdrawing, weighing, necropsy, anesthesia, euthanization, surgery and measurement of ECG, respiratory function and CNS FOB and test,

　　Record observations and collect other relevant data via data acquisition system and hand-generated

　　Report to technical supervisor or Study Director in a timely manner regarding any deviations from protocols or unexpected

　　Contribute to quality control the raw data from studies.

　　Requirements:

　　1.

　　 degree in life science or diploma in life science with strong animal work and /or surgery skills 2.

　　Work experience in related fields preferred 3.

　　Basic lab and animal work skills are required.

　　组织病理学实验室技术人员

　　组织病理学实验室主要从事GLP实验中组织切片的制备。

　　职位要求：

　　1.

　　病理学、兽医学、实验动物医学或医学专业本科或硕士； 2.

　　有病理技术工作经验优先； 3.熟练操作计算机能力； 4.

　　良好的英语读写能力；

　　5.

　　优秀的团队精神、工作踏实，具有较强事业心。

　　Histopathology Technicians participate in the technical aspects of cell and tiue-based visualization aays in support of preclinical research and development will aist the pathologist and be supervised by the head of histopathology to proce histological slides for histopathologic evaluations.

　　Responsibilities will include 1.

　　Identify tiues preserved in formalin solution and trim the preserved tiues for histopathology slides.

　　2.

　　Prepare paraffin tiue blocks and handle the microtone instrumentation during slide preparation. 3.

　　Will also involve in the handling of instrumentation for dehydration and staining.

　　4.

　　Frozen tiue sectioning

　　5.

　　Immunostaining and conjugation of antibodies an and proteins with biotin and/or dyes

　　6.

　　Microscopy and digital imaging

　　7.

　　Ensure all job aignments are performed in compliance with GLP regulations

　　Qualifications and Experience 1.

　　BS or MS in biological science, preferably molecular and cell biology or biochemistry

　　2.

　　Experience in histology/pathology laboratory work with animal models is preferred

　　3.

　　Previous experience with immunofluorescence and multi-target detection methodologies preferred

　　4.

　　Must be able to work in small group setting

　　Pharmacologist /Aociate III, Pharmacology– Beijing, PRC

　　The Pharmacologist or Aociate III, pharmacology will adhere to Pharmaron SOPs, comply with GLP, ICH and other guidelines and maintain the highest standards to ensure the integrity of preclinical study the guidance from the Director of Pharmacology, the individual will be responsible for preclinical pharmacology, safety pharmacology and related safety studies.

　　Responsibilities will include but not limited to: 1.

　　Development of various disease models and technical procedures for study

　　Act as study director for pharmacology, safety pharmacology and related safety

　　Provide data and analysis for study reports 4.

　　Prepare study protocols and study reports Qualifications and Experience: 1.

　　MS or PhD in life sciences

　　2.

　　Experience in animal ECG or surgery preferred 3.

　　Knowledge of regulatory requirements 4.

　　Able to use English for work activities