「[全職]臨床研究護理師CRN-萬芳醫院」的相似工作

1.提供基本基礎醫藥照顧， 如：給、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）、進食量、排便狀況等。 3.撰寫護理表單，如：ADL、IADL、MMSE、SPMSQ等。 4.觀察、記錄並回報個案狀況，如有不尋常的症狀反應，採取救護措施。 5.協助個案開案評估。 6.緊急事件應變處理。

臨床試驗 1. 臨床試驗收案、講解同意書。 2. 問卷訪談填寫、資料key-in。 3. AE事件通報。 4. 有研究護士等相關經驗/背景者尤佳

（有CDE衛教師資格） 1.能提供專業健康檢查包括靜脈肌肉注射、協助服藥與衛生教育等護理臨床工作 2.教育民眾各種醫藥常識、提供慢性病照護（包括胰島素注射及相關儀器檢測） 3.疫苗管理及疫苗常識衛教追蹤 4.批價掛號等院所相關行政管理業務,社群網站管理 5.緊急(意外傷害)應變處理 6.相關檢查儀器操作及使用 7.團體衛教活動的設計及執行 8.急慢性相關護理衛教指導 9.慢性病(糖尿病、腎臟病等)專案管理行政作業及公自費疫苗管理 10.參與各個學會舉辦的活動及計畫

1.日照個案收托及管理評估 2.個案用藥、疾病管理 3.緊急/意外傷害應變處理 4.個案健康管理及定期護理需求評估，擬訂照護計畫並執行相關紀錄 5.執行健康促進活動及家屬衛教、護理諮詢 6.指導照顧服務員長者照顧與技巧 7.感染控制與預防 8.協助機構評鑑相關事宜 9.行政會議參與及其他主管交辦日照相關事項 工作地點:雙北、新竹、高雄，依人力需求及應徵者意願協調安排

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.

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

【 你會要做什麼呢？】 1.配合健康檢查預約業務，依照SOP完成各項檢查作業 2.正確操作各項儀器設備 3.提供客戶檢查前中後相關護理指導及說明 4.列印檢查報告，交由該科負責醫師判讀後核發報告 【 你要具備什麼呢？ 】 1.具備護士或護理師證書，符合執業資格可以執業登錄 2.期待您具備以下資歷或特質，將優先錄用： (1)有醫院臨床工作或健檢中心資歷者 (2)具職業衛生護理研習證書者 (3)已接受BLS之訓練課程者 (4)積極負責、個性開朗、溫和有禮、儀態大方，具高度服務熱忱者 【 薪資待遇 】 (1)月薪區間：本薪39,000-45,000元；每月另有伙食津貼，按季發放。 (2)如有達成推廣之業績目標與獲得客戶肯定，將依據個人績效表現達標情形，另外發放達標之業績獎金、顧客滿意度獎金。 (3)年終(績效與考績獎金)另計，依據獲利程度、個人績效及組織目標達成率決定獎金發放金額。 備註：此職缺有兩個班別（7:30-16:00 / 8:00-16:30），並需配合週六開診需求。投遞前請先確認是否能接受此時段安排，感謝您的理解！

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

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。

1.安排受試者回診及進行相關檢查 2.收集檢測結果及資料整理 3.填寫個案報告表及完成相關文件 4.協助醫師依院內規定通報藥品相關不良反應 5.觀察受試者不良事件反應 6.作為受試者與試驗醫師之溝通橋樑 7.協助及配合臨床試驗監測與稽核 8.依臨床試驗計畫書, 藥品優良臨床試驗準則(GCP)及相關法規執行臨床試驗 9.主管交辦事項

1. 醫美產品之教學與技術示範 2. 配合醫師進行療程跟診相關作業 3. 口條清晰佳 4. 協助業務代表了解醫師需求並展示設備。 5. 適應力高及抗壓能力強，具團隊合作精神者，無相關經驗者可，但須有高度學習企圖心。 6. 具護理師資格（會注射17G針頭） 7. 其他主管交辦工作。

Brief Position Description: The Site Management Associate (SMA) is responsible for planning, directing, and managing clinical trials at site. The SMA also implements remote site management activities according to the Site Management Plan, ensuring that clinical trials are conducted and documented, as per protocol, ICH GCP guidelines and applicable regulatory requirements and SOPs. 工作內容: 1. 協助醫師執行臨床試驗計畫 2. 完成資料及試驗數據之收集、記錄 3. 有研究護理師經驗者佳 4. 計畫及管理臨床試驗 5. 執行試驗場地管理 (依據試驗場地管理計畫) 6. 確保臨床試驗的執行及紀錄，是依據ICH GCP準則、本地及全球性的法規要求、諾佛葛及試驗場地的標準作業程序 Reporting to: As indicated on current organisation chart. Responsibilities: Conduct and complete remote site management activities and/or on-site visits according to the Site Management Plan. Specific duties include: Serve as a primary point of contact for site communication. Implement study start-up activities including but not limited to gathering feasibility information, negotiation of contract and budgets, planning for subject recruitment, communication with IRB/IEC. Collaborate with the principal investigator to prepare IRB/IEC and any other regulatory submission documents as required per protocol, ICH-GCP and local regulations. Ensure amendments to an approved protocol, informed consent form, and other relevant documents are submitted to IRB/IEC for approval as required and assure that changes are not implemented prior to approval. Arrange with monitor the scheduled date, time and location of site initiation visit. Prior to the site initiation visit, review the Investigator's Brochure and any up-to-date information on the investigational product for assessment of risk/benefit ratio of study participation in order to set Site Management Service Plan. Perform study-related tasks delegated by the principal investigator within the contracted scope. SMA is responsible for performing tasks appropriate for its role, unless otherwise noted on a protocol specific delegation of authority log. Support the investigator to identify suitable subjects for screening according to the eligibility criteria. If necessary, assist the principal investigator to use directed and IRB/IEC approved advertising (newspaper, TV, Internet advertisements, posters, etc.) materials. Provide written and verbal site updates on study progress to the line manger according to the study requirements/timelines. Ensure adequacy of information and data contained in site visit reports and other site management documents. Manage the site expenses of clinical trial including but not limited to subject reimbursement, material cost, travelling expense, cost for technical information, utilities and fees.

Please do submit English resume to our company website. https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2683/?utm_medium=jobshare Brief Position Description: The Study Nurse is responsible for planning, directing, and managing clinical trials at site. The Study Nurse also implements remote site management activities according to the Site Management Plan, ensuring that clinical trials are conducted and documented, as per protocol, ICH GCP guidelines and applicable regulatory requirements and SOPs. Reporting to: As indicated on current organisation chart. Responsibilities: Conduct and complete remote site management activities and/or on-site visits according to the Site Management Plan. Specific duties include: Serve as a primary point of contact for site communication. Implement study start-up activities including but not limited to gathering feasibility information, negotiation of contract and budgets, planning for subject recruitment, communication with IRB/IEC. Collaborate with the principal investigator to prepare IRB/IEC and any other regulatory submission documents as required per protocol, ICH-GCP and local regulations. Ensure amendments to an approved protocol, informed consent form, and other relevant documents are submitted to IRB/IEC for approval as required and assure that changes are not implemented prior to approval. Arrange with monitor the scheduled date, time and location of site initiation visit. Prior to the site initiation visit, review the Investigator's Brochure and any up-to-date information on the investigational product for assessment of risk/benefit ratio of study participation in order to set Site Management Service Plan. Perform study-related tasks delegated by the principal investigator within the contracted scope. Study Nurse is responsible for performing tasks appropriate for its role, unless otherwise noted on a protocol specific delegation of authority log. Support the investigator to identify suitable subjects for screening according to the eligibility criteria. If necessary, assist the principal investigator to use directed and IRB/IEC approved advertising (newspaper, TV, Internet advertisements, posters, etc.) materials. Provide written and verbal site updates on study progress to the line manger according to the study requirements/timelines. Ensure adequacy of information and data contained in site visit reports and other site management documents. Manage the site expenses of clinical trial including but not limited to subject reimbursement, material cost, travelling expense, cost for technical information, utilities and fees.

1.負責臨床試驗行政流程工作 2.協助按照臨床試驗計劃書完成相關流程 3.講述知情同意書及程序，並協助受試者招募、篩檢和安排檢查以及臨床試驗執行 4.臨床試驗收案監測、收案進度追蹤、試驗品質掌控與管理(彙整文件與歸檔)。 5.臨床試驗資料之分析彙整與會報。 6.協助臨床試驗稽核與查核及報告。 7.不良事件和嚴重不良事件通報 8. 確保試驗中心品質 9. 協助臨床醫師進行臨床是數據分析 10.部門主管或專案負責人交辦事項 11.有研究護士等相關經驗/背景者尤佳 【工作地點】臺大醫院 【工作待遇】依據國立臺灣大學計畫專任研究助理支給參考表；可依年資調整；享勞健保、年終獎金。

1. 需具備護理師證書證照 2. 醫學門診及跟診：協助醫師執行各項預防醫學療程治療及術後衛教 3. 守護顧客健康：針對顧客健康，進行相關項目諮詢介紹或追蹤檢後狀況與提供衛教建議 4. 貼心關懷護理：進行貼心與關懷之IV與護理相關工作。 5. 熟IV注射 6. 有預防醫學、再生醫學、醫學美容、皮膚科或整形外科經驗者佳。

工作內容 1. 需具備護士或護理師證書(不需職登) 2. 協助門診醫師--收案/衛教/健保文書作業/個案管理/不良事件通報 工作時間 週二 上午診 週三 上午診 週六 上午診 公司福利 勞健保.勞退.津貼.獎金.福委福利.年終.在職訓練

**全台第一家牙醫醫院** 1、醫院感染管制業務暨相關教育訓練、查核。 2、配合年度督導考核業務及醫院評鑑感染管制章節之統整查核。 3、各項感染管制相關指標及統計分析。 4、感染管制相關業務推動及執行(如：稽核無菌技術操作、員工流感疫苗、洗手宣導…等) 5、感染管制委員會執行。 6、院內、外相關單位之協調與業務諮詢。 7、教學與研究。 8、主管交辦事項

臨床新航線：從醫療前線到醫學科普的內容戰場！ 你在臨床累積了豐富的醫療經驗， 卻發現自己更喜歡用文字和創意， 向大眾傳達正確又有趣的醫學知識？ 這一次，換你掌握衛教的話語權！ MD cafe 醫識咖啡正在找尋一位熱愛醫學科普的你， 結合你的臨床實務經驗， 與我們一起打造最具影響力的醫療衛教平台。 你的任務包括： 1. 策劃與製作專業卻深入淺出的醫學內容 2. 經營社群，拉近與用戶的距離 3. 協作多媒體團隊，創造更多元的互動體驗 4. 支援行銷活動，讓內容更具影響力 5. 追蹤內容成效，提出優化建議 你需要擁有： 1-2年臨床工作經驗 對醫學科普的熱情與好奇心 願意嘗試新的內容創作與行銷模式 如果你希望用另一種方式守護大眾健康， 現在就加入我們，一起讓醫療知識成為日常對話！ 點擊投遞履歷，開啟你的全新醫學科普之路！

必要條件資格說明 1. 大廠專職專任勞工健康服務護理師資格3年以上 2. 特約勞工健康服務護理師，資格3年以上 ~特約臨場服務事業單位端執行臨場服務工作~ 1.勞工之健康教育、健康促進與衛生指導之策劃及實施 2.依勞工健康保護擇規則辦理健康促進活動 3.職業病預防及分析管理 4.職業衛生之報告及傷害、疾病紀錄之保存 5.客戶年度健檢諮詢、 健檢報告衛教 6.員工意外事件預防、急救處理、照護及追蹤關懷 7.協助職業安全衛生相關工作及報表處理 8.其他主管交辦事項

*需具備護士或護理師執照。 *需具備醫美護理師經驗者。 工作內容: 1、醫學術後保養，卸洗、護理工作。 2、雷射治療術前術後衛教、卸洗，上麻，護理、解說。 3、皮膚醫療相關護理工作 (跟診、注射、抽血等)。 4、健保跟診。 5、病歷文件檢查及核對。 上班時間： 週一~週五 午班: 13:00~17:00 4小時 ，晚班: 17:30-20:30 3小時， 週六 早班 10:00-13:00 3 小時，午班 13:30 ~17:30 4小時 PT時間 ，需要全天，每小時時薪250，每週至少三天。