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1704 筆查詢結果

Clinical Research Associate

FULL_TIME
台北市大安區
新加坡商希米科亞太股份有限公司台灣分公司
  • 碩士以上
  • 一年以上工作經驗
  • 待遇面議
1、Responsible for clinical research tasks relating to the sites in charge, conducted in CMIC such as monitoring, filing and reporting. 2、Responsible to confirm that the assigned study is conducted in line with the relevant regulatory requirements/procedures, e.g. applied GCP, local regulations/rules, SOP.
6天以前更新 兩週內6-10人應徵
2022-01-11

Senior Clinical Research Associate

FULL_TIME
台北市信義區
台灣米高蒲志國際股份有限公司
  • 大學
  • 三年以上工作經驗
  • 待遇面議
• Top 10 global Pharma permanent headcount • Strong pipelines and clinical research team About Our Client Our client is a top-ranking MNC pharma who develops and produces medicines, vaccines, biologic therapies and animal health products, with outstanding market share in cancer immunotherapy, anti-diabetic medication and vaccine Job Description • Join and maintain study site selection, monitorin
4天以前更新 兩週內0-5人應徵
2022-01-13

Senior Clinical Research Associate

FULL_TIME
台北市中山區
瑞士商艾伯維藥品有限公司台灣分公司
  • 大學以上
  • 三年以上工作經驗
  • 待遇面議
• For assigned sites/study(s), ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out. Ensure site related study execution including but not limited to monitoring visits, site evaluations, site selection, and activation, and monitoring close out and visit reports. Anticipate and identify site issues that could affect timelines and develop altern
兩個月以前更新 兩週內0-5人應徵
2021-11-01

In House Clinical Research Associate

FULL_TIME
台北市中山區
諾佛葛生技顧問股份有限公司
  • 大學以上
  • 工作經驗不拘
  • 待遇面議
Responsibilities: Support the clinical team’s inhouse activities on assigned projects. Co-ordinate and maintain clinical study documentation in the Trial Master Files (TMF) including the tracking of documents, preparation for internal/external audits, conducting routine QC reviews and final reconciliation, according to the requirements of ICH GCP and Novotech (or client) SOPs. Support the clinica
5天以前更新 兩週內0-5人應徵
2022-01-12

Research Associate (DMPK)

FULL_TIME
台北市南港區
台灣微脂體股份有限公司
  • 大學以上
  • 二年以上工作經驗
  • 待遇面議
1.. Responsible for the clinical/preclinical PK data calculation, interpretation, integration and reporting 負責臨床/非臨床試驗藥物動力學數據計算、統整說明及報告撰寫。 2.. Prepare PK components of clinical & preclinical study protocol designs and reports. 負責臨床/非臨床試驗計畫書中藥物動力學相關之試驗設計及報告。 3.. Manages the clinical/preclinical study budget, ensuring project remains
5天以前更新 兩週內0-5人應徵
2022-01-12

Research Associate (SIF)

FULL_TIME
台北市南港區
逸達生物科技股份有限公司
  • 碩士以上
  • 一年以上工作經驗
  • 待遇面議
• Formulation development of sustained release dosage forms including solutions, suspensions, micro- or nanoparticles, and implantable products. • Preparation and characterization of test articles in support of in-house and collaborative programs. • Planning and performing laboratory experiments to develop and optimize formulations and manufacturing processes. • Generation and testing of formulati
6天以前更新 兩週內0-5人應徵
2022-01-11

(Senior) Clinical Research Associate

FULL_TIME
台北市松山區
IQVIA_艾昆緯股份有限公司
  • 大學以上
  • 二年以上工作經驗
  • 待遇面議
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. On
2天以前更新 兩週內0-5人應徵
2022-01-15
諾佛葛生技顧問股份有限公司
  • 大學以上
  • 三年以上工作經驗
  • 待遇面議
Clinical Research Associate II - Clinical Research Associate III-Senior CRA Position Description: Responsible for monitoring and managing the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), Study Specific Procedures (SSP), and applicable regulatory requirements. Responsibilities: • Performing site evaluation, initiation, monitoring and close-out visits, p
一週以前更新 兩週內0-5人應徵
2022-01-07

Clinical Research Associate I

FULL_TIME
台北市中山區
諾佛葛生技顧問股份有限公司
  • 大學以上
  • 工作經驗不拘
  • 待遇面議
Brief Position Description: The Clinical Research Associate I role is a CRA entry level training position. The CRA I will learn the company culture, policies and procedures through a specialised training program; and on the job training by supporting the day-to-day operations of clinical projects and project team members such as Clinical Research Associates (CRAs) and Project Managers (PMs), in
一週以前更新 兩週內11-30人應徵
2022-01-07
台灣璞氏健康發展有限公司
  • 大學以上
  • 三年以上工作經驗
  • 待遇面議
Job description: • Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits • Site management, general administration of clinical research studies • Contact for clinical investigators, vendors and support services in regard to study progress • Monitoring trial progress and ensuring that the project timelines are met • Facilitation of site budgets
6天以前更新 兩週內0-5人應徵
2022-01-11
ICON_保瑞爾生技股份有限公司
  • 大學 碩士
  • 一年以上工作經驗
  • 待遇面議
Clinical Research Associate Location: [Taiwan] 對於喜歡快速得到sponsor反饋的你,千萬別錯過FSP的CRA機會,你將在sponsor的辦公室工作,迅速的得到一手的回饋。 對於目前只在core team工作的你,也能夠嘗試不同的工作模式,拓展在臨床領域的工作經驗。 目前有多個不同的工作地點(藥廠),能夠提供你做嘗試,歡迎您應徵或加入我們的line@做更進一步的討論。 Providing innovative solutions for our clients is what we do. Bu
5天以前更新 兩週內0-5人應徵
2022-01-12
ICON_保瑞爾生技股份有限公司
  • 大學 碩士
  • 二年以上工作經驗
  • 待遇面議
Clinical Research Associate Location: [Taiwan] Providing innovative solutions for our clients is what we do. But innovation just for the sake of innovation isn’t why we do it. Side-by-side with our clients, we strive to move drug discovery forward, to help them develop life-saving and life-improving drugs. We help change people’s lives for the better every single day. It’s who we are. And it’s
5天以前更新 兩週內0-5人應徵
2022-01-12

Senior Clinical Research Associate

FULL_TIME
台北市信義區
美商默沙東藥廠股份有限公司台灣分公司
  • 大學以上
  • 二年以上工作經驗
  • 待遇面議
- Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. - Gains an in-depth understanding of the study protocol and related procedures. - Coordinates
5天以前更新 兩週內0-5人應徵
2022-01-12
臺灣阿斯特捷利康股份有限公司
  • 大學 碩士
  • 二年以上工作經驗
  • 待遇面議
- Be responsible for initiating, organizing and managing the assigned studies. - On site monitoring and site managements for global studies. - Ensure clinical trials conducted in compliance with protocol & GCP. - Ensure clinical trials can be conducted per timeline requirement.
一週以前更新 兩週內11-30人應徵
2022-01-10
台灣雙健維康生技顧問有限公司
  • 大學 碩士
  • 五年以上工作經驗
  • 待遇面議
- Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. - Proform study monitoring visits and site management for a variety of protocols, sites and therapeutic areas. - Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing proj
1小時以前更新 兩週內0-5人應徵
2022-01-17
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