「[全職]臨床研究護理師CRN-萬芳醫院」的相似工作

家醫科診所，一般門診業務。 1. 門診掛號。 2. 接聽病患求助電話、慢性病返診提醒。 3. 協助診間運作。 4. 急慢性病症衛教。 5. 急慢性病抽血、成人健檢，需熟練抽血！！！ 6. 肌肉注射。（極少量，醫師不愛打針） 7. 觀察病人候診及診療前後之狀態，特別是一些不尋常的症狀反應，並即時回報。

本職缺僅接受國泰人壽徵才網站的履歷表，請至以下網址登錄您的資料：『https://pse.is/3ys9f7』，謝謝！ 1.依勞工健康保護規則及職業安全衛生相關法規事項執行。 2.勞工健康檢查結果之分析與評估、執行四大計劃與追蹤管理。 3.辦理健康講座及員工健康促進活動。 4.醫護臨場服務規劃、執行與管理。 5.員工健康諮詢與疾病預防宣導。 6.協助辦理健康促進相關專案。 7.需出差，一年累積時間一個月內。 8.其他主管交辦事宜。

跟診、檢驗、跟刀及衛教咨詢 一般行政工作 接聽病患求助電話，並且提供協助。 指導病患居家自我療護，如：術前術後衛教，並且提供相關諮詢。 協助醫師門診作業及檢查。 疾病護理相關衛教說明。

1. 從事專業護理服務工作、跟診、衛教、健撿程序、IM、IV、抽血 等。 2. 協助櫃檯(營收結帳、接電話、預約、掛號)及行政工作 成就樂趣： 提供正確的醫療方針和觀念是我們的志向 我們要給予專業的醫療服務也要保有專業的醫療尊嚴 希望可以找到志同道合的工作伙伴 員工福利: 三節禮金, 年終獎金, 員工聚餐, 慶生會. 尾牙,員購優惠,專業課程

1. 負責健康諮詢與關懷服務，強化職場健康照護與支持機制。 2. 定期辦理員工健康檢查，負責健檢安排、資料記錄與保存與管理、個案追蹤等作業。 3. 規劃勞動部職安署四大健康促進計畫，保制度符合法規並有效落實。 4. 推動健康職場政策，辦理健康課程或講座。 5. 提供法令規範所需之行政服務事項。

ICON公司為全球前五大CRO 臨床試驗機構，全球第一大FSP公司，與全球頂尖的藥廠合作，提供專業的臨床研究服務。 提供員工良好且完整的教育訓練，透明的升遷制度，完善的休假制度，周休二日，讓員工能在良好的支援下為世界提供更新、更好的新藥品。 臨床試驗專員 1.藥品臨床試驗計畫啟動至結案過程的觀測及監督。 須具備良好的溝通能力以及敏捷的緊急應變能力，能跟試驗單位進行良好的溝通，並協助案件進行。 2.臨床試驗相關個案報告整理。須具備良好的檔案管理能力。 3.工作型態：需要出差到試驗單位(醫院)，查看臨床試驗的進度，並定期回報給專案經理，確認試驗持續符合計畫案的里程碑。出差天數依據試驗案的進程而定。 4.具備良好的英文讀寫能力，所有公司文件皆以英文撰寫。 5.目前需要具備一年以上的臨床試驗案進行經驗的人才。職級及薪水的核定將以面試來決定。面試有兩關，約在兩周內就會完成。 6. 歡迎持有身心障礙證件者投遞 Responsibilities The Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. Key responsibilities include: 1. Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out. 2. Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan. 3. Develop effective relationships with investigator site staff to ensure that key clinical metrics are met. 4. Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies, and following up on drug safety issues. 5. Ensuring the integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines 6. Negotiation and ongoing management of clinical trial agreements with investigative sites.

誠徵第三位護理師，自費獎金另計，薪資依年資及工作表現增加，有醫院經歷優先，歡迎態度積極良好，工作配合度高，有自費熱忱的人才加入！ 如兼職或半職也可以面談

1.負責勞工之健康教育、健康促進與衛生指導之策劃及實施、進而促進同仁健康 2.負責職業傷病及一般傷病之防治、健康及醫療諮詢、急救及緊急處置送診、照護及追蹤 3.負責協助雇主選配勞工從事適當之工作(職災工傷期間) 4.負責辨識與評估工作場所環境、作業之危害及緊急應變 5.負責勞工體格、健康檢查紀錄之分析、評估、管理與保存及健康管理、個案追蹤管理 6.負責職業衛生之傷害、疾病紀錄、職災調查報告之保存分析 7.負責協助雇主與職業安全衛生人員實施職業病預防及工作環境之改善 8.負責臨場服務協助，包含數據分析與規劃溝通與追蹤 9.其他主管機關及主管交辦事項 *代理期間(至114.12.31)

This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer. Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. Responsible for all aspects of site management as prescribed in the project plans. General On-Site Monitoring Responsibilities. Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data. Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy. Ensure audit readiness at the site level. Travel, including air travel, may be required and is an essential function of the job. Prepare accurate and timely trip reports. Interact with internal work groups to evaluate needs, resources, and timelines. Act as contact for clinical trial supplies and other suppliers (vendors) as assigned. Responsible for all aspects of registry management as prescribed in the project plans. Undertake feasibility work when requested. Participate in and follow-up on Quality Control Visits (QC) when requested. Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned 18) Assist Senior CRA with managing investigator site budgets. Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management. Assist with training, mentoring and development of new employees, e.g., co-monitoring. Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned. Perform other duties as assigned by management. Qualifications (Minimum Required): University or college degree in a related allied health profession from an appropriately accredited institution. Basic knowledge of Regulatory Guidelines. Basic understanding of the clinical trial process. Fluent in local office language and in English, both written and verbal. Experience (Minimum Required): 2 years CRA experience with on-site monitoring experience. Oncology trial experience is MUST. Basic understanding of Regulatory Guidelines. Ability to work within a project team. Good planning, organization, and problem-solving skills. Good computer skills with good working knowledge of a range of computer packages. Works efficiently and effectively in a matrix environment.

1.醫美療程諮詢衛教。 2.客戶接待管理。 3.術前術後諮詢。 4.提供專業建議與保養服務。 5. 協助執行業務推廣 6.須具備護理師執照 7.具醫美銷售經驗

1.員工急救/傷病照護、協助/陪同就醫 2.員工健康促進相關活動規劃執行、異常追蹤、廠醫臨廠服務 3.醫療耗材管理、盤點、採購 4.HR/福委相關活動辦理及其他主管交辦事項

【醫院/診所名稱】 藍海曙光 杏誠復健診所 藍海曙光 永誠復健診所 宏恩綜合醫院復健科 徵才條件： 具備物理治療師證書（應屆畢業通過國考者可） 【薪資/福利待遇】 月薪約 52,000，業績達標後另有業績獎金 物理治療師公會 年費補助 三節獎金 藍海學苑課程費用補助 規律的排班與休假，沒有兩頭班、花花班。 完整的專業訓練 不定期集團旅遊、年度活動 【單位介紹】 杏誠復健診所臨近信義安和捷運站，永誠復健診所臨近科技大樓捷運站，宏恩綜合醫院臨近忠孝復興捷運站，皆為規劃完善、制度完備並具規模之復健治療中心。 我們擁有醫學中心級的醫師與多位資深物理治療師執業，並自民國99年起，均榮獲台北市早療機構評鑑優等以上的殊榮。個案類型涵蓋骨骼肌肉系統損傷、神經疾患與小兒個案，健保與自費皆有發展空間 我們重視人員專業能力的發展，定期舉辦在職教育與專業訓練，含國內外研討課程與徒手工作坊，如「AMT進階肌筋膜徒手徒手技巧研討會與工作坊、肩關節研究新知與徒手治療、肌能系貼紮認證課程、ICB鞋墊製作」，學習各項國際精進技術與新知。員工『提供藍海學苑相關課程的費用補助』。致力培養可獨當一面的治療師。透過接觸不同種類的個案與繼續教育課程，讓你進入職場兩年後脫胎換骨，變成新的自己！ 【歡迎加入我們】 請您於以下網址下載制式徵人專用履歷表https://www.hnl.com.tw/articles.php?contactus 填寫完畢後以附加檔案方式寄至[email protected] 信件主旨請載明「【應徵PT】○○○（姓名）履歷表」， 例如「【應徵PT】王大明履歷表」，並於信件當中註明應徵藍海曙光集團 物理治療師之職缺 我們會在收到履歷後24小時內回信告知已收到您的資料。 如有任何問題，歡迎來訊詢問，我們將全力安排您的面試，謝謝！

【工作內容】 1.須具備中華民國護理師執照並配合執業登記 2.熟稔抽血與輸液治療 3.醫師跟診 4.服務項目諮詢,衛教及追蹤 5.診所環境值日生輪值 6.主管交辦事項 【加分項目】 有醫美診所經驗者佳 【獎金】 1.執業獎金 2.績效獎金 3.年終獎金 4.三節獎金 【福利】 旅遊假

1. 協助醫師看診、跟診及相關準備工作。 2. 提供病患基礎醫藥照顧，如：包紮傷口、換藥等。 3. 進行抽血、靜脈注射、肌肉注射、打點滴，觀察記錄給藥狀況。 4. 慢性病等病患追蹤管理及衛教說明。 5. 器械消毒及清潔準備。 6. 耗材盤點及請購、設備維護。 7. 接待病患及櫃台掛號及相關行政作業 8. 具電腦操作基本操作。 9. 協助處理診所相關醫療事務，及其他主管交辦事項。 10. 有診所/醫院護理經驗者為佳 本診所工作環境優、周休二日、三節及年終獎金、歡迎專業且熱忱的護理伙伴加入！※依學經歷、工作年資敘薪

1.提供基本的病患基礎醫藥照顧， 如：跟診 包紮傷口、換藥等。 2.測量並且記錄病患的生理狀態（如：體溫、血壓、脈搏和呼吸）檢查儀器操作。 3.進行靜脈注射、肌肉注射、打點滴，觀察記錄患者給藥之後的狀況並加以回報。 4.觀察、記錄並回報病人在接受醫療後狀態的改變，特別是一些不尋常的症狀反應，必要時採取措施。 5.文書處理及系統操作，接聽病患電話，並且提供協助。 6.基本院內清潔 7.慢性病專案衛教

CRA for BE study/New drugs/Medical devices 1.Clinical research study setup/study procedure setup/site staff training 2.Site monitoring visits/source data verification/deviation reporting in compliance with GCP 3.Trial documents maintenance/regular site visits and maintenance/study materials supply/interim reports 4.regular report to sponsor/communication between sponsor and site. 5.site close-out/trial materials retrieval 6.audits/regulatory inspection participation upon request

*此為Adecco外包職缺，合約期間一年** *歡迎將履歷郵寄至[email protected] 【Job Purpose】 PSP manager is responsible for optimizing PSP vendor profile for potential new coming solutions, and improve program’s impact and efficiency, aligning with companys vision and patient-focused approach, as well as global and local related policy. Support driving PSP excellence. 【Major Accountabilities】 As SQA Manager and ESP management (strategic ESP contract and ESP optimization)  Responsible for the overall management of the External Service Providers (ESPs), being the main point of contact and ensuring the following activities are completed prior to the beginning of ESP services: - Conduct of POP Supplier Quality Assessment (SQA) and other supplier qualifications, including Information Security and Risk Management (ISRM), External Partner Risk Management Assessment (EPRM), Anti-Bribery, etc. - Contract management and execution, including Pharmacovigilance and data privacy language - Ensure ESP AE training completion  Collaborate with different stakeholders to onboard, manager ESPs and support assess the performance and compliance of ESP, and provide the recommendations for subsequent actions  Ensure compliance with all applicable local laws and regulations  Provide support during internal and external audits and inspections as required

1. 執行臨床試驗相關業務，包含試驗前準備、臨床收案、受試者追蹤，及試驗資料管理等； 2. 協助研究倫理委員會送審、管理臨床研究資料； 3. 協助計畫相關行政作業，例如計畫審查作業等； 4. 其他研究主持人交代事宜。

招募熱忱且細心的研究助理，加入我們的實驗室，支援研究與實驗工作，並協助維持實驗室日常運作。主要工作內容如下： 1. 協助進行科學研究與生物實驗 2. 整理並分析實驗數據 3. 文獻查詢、彙整與報告撰寫 4. 協助實驗室管理與採購 5. 指導學生進行實驗操作 6. 協助撰寫研究計畫與成果報告

一、工作內容： 1.精iv，跟注射。 2.維護工作環境整潔、器械保養消毒。 3.負責術後關懷及術後衛教。 4.執行手術室護理。 5.依照診所標準作業流程執行護理業務。 6.協助醫師執行醫療業務。 7.恢復室照護。 8.有耐心、有笑容提供客人溫馨、舒適的醫療服務。 9.需醫療美容工作相關者 10.需開刀房經驗。 二、獎金 1、業績團體獎金 2、年度盈餘年終獎金 3、三節獎金 三、福利: 1、提供勞健保/年度休假 2、免費新進員工教育 3、提供免費員工制服 4、提供免費在職訓練、教育訓練 5、員購福利:員工購物享有員工價 6、生日禮金 所需特質： 1.具團隊合作精神 2.情緒控管、抗壓性強 3.正面思考 4.樂觀積極 5.有責任感 6.執行力強 7.具備親和力與行銷能力 8.思考靈活及良好操守 9.高服務熱忱 職涯規劃： 員工三年培訓計畫培訓升職主管至診所合夥人一起團隊打拼

Working location: ICON office, fully office based. **No flexible to work from home. What you will be doing: • TMF filing, quality, maintenance, compliance, and oversight • Development and delivery of sites’ ISF, and eISF when utilized, and act as primary point of contact for the sites and manage the Site Operations/monitor access to eISF prior to SIV • Maintain sponsor Registries and systems as required • Provide reporting to support management of clinical trials • Provide support with audit and inspection readiness activities • Perform customization and translation of documents as required • Preparation of documents and communications for distribution to and collection from sites, as required • Manage physical printing, shipping and archiving needs as required • Contribute team project and initiative at country or regional level • Provide technical and operational support to the study team members from study start up to study close out • Support of site payment services, patient compensation services and other local payments as required • Works proactively and independently to coordinate and prioritize multiple key tasks at site, country and study level. • Serve as SME for key CTA processes, systems and tasks. • Collaborates with regional or local cross functional study team members of varying levels of seniority. • Use established procedures and methodologies to ensure the completion of assigned tasks according to timelines and to required quality standards. • Perform the assignments by supervisors • Be agile and flexible in adapting to the changes in work scope according to business needs <For Senior level> • Provide support to managers for development and implementation of on-board training for new hires • Work with managers to identify continuous improvement opportunities to enhance operational efficiencies. • Gathers and retains knowledge of local processes that enable clinical trial execution where required. • Lead the development and delivery of sites’ ISF, and eISF when utilized, and act as primary point of contact for the sites and manage the Site Operations/monitor access to eISF prior to SIV

1. 協助尋找受試者及聯絡事宜 2. 協助解釋試驗內容及受試者同意書填寫,體檢相關事宜 3. 協助試驗前場地佈置,用物準備，儀器維護，相關事宜聯繫 4. 協助試驗執行 5. 協助試驗結束後受試者體檢及營養費發放 面試地點：新北市汐止區新台五路一段104號7樓(明生總公司) 工作地點一：台北市中山區中山北路一段72號2樓(明生診所) 工作地點二：台北市中正區忠孝東路一段138號11樓(鍍生生技)