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1203 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.
2天以前更新 兩週內11-30人應徵
2019-10-14

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
一週以前更新 兩週內0-5人應徵
2019-10-08

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
一週以前更新 兩週內6-10人應徵
2019-10-08
香港商法馬蘇提克產品發展有限公司台灣分公司
  • 大學以上
  • 一年以上工作經驗
  • 待遇面議
Description Basic Purpose and objective: Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Repre
兩個月以前更新 兩週內0-5人應徵
2019-06-18
台灣愛康恩研究有限公司
  • 專科以上
  • 一年以上工作經驗
  • 待遇面議
- Primary point of contact between site staff and the company. Acts as ambassador for the company and contributes to making company the preferred partner. - Responsible for taking leadership of site management for the selection and initiation of sites as well as conduct and closing activities of the appointed studies in compliance with local regulations, ICH- GCP, company procedures and protocol
一個月以前更新 兩週內6-10人應徵
2019-09-11
佳生科技顧問股份有限公司
  • 大學以上
  • 二年以上工作經驗
  • 待遇面議
1. Conduct remote feasibility survey and on-site evaluation visit to evaluate potential sites and provide recommendations for selection of qualified sites. 2. Develop country/site specific ICF according to the core study ICF. 3. Perform site budget estimation and prepare/manage the clinical trial agreements with investigators/sites. 4. Assist investigator meeting conduction. 5. Demonstrate st
一週以前更新 兩週內11-30人應徵
2019-10-04

Clinical Research Associate (CRA)

FULL_TIME
台北市信義區
PRA Health Sciences_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] 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
1小時以前更新 兩週內11-30人應徵
2019-10-16
PRA Health Sciences_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] 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
1小時以前更新 兩週內0-5人應徵
2019-10-16
科文斯諮詢服務股份有限公司
  • 大學 碩士
  • 二年以上工作經驗
  • 待遇面議
Our Flexible Solutions Clinical Research Associates are based at our pharmaceutical client sites and manage all aspects of study site monitoring according to Client SOP, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. Responsibilities include: •Study startup which include IRB/IEC
2天以前更新 兩週內6-10人應徵
2019-10-14

Clinical Project Associate

FULL_TIME
台北市信義區
西藥_羅氏大藥廠股份有限公司
  • 專科 大學
  • 三年以上工作經驗
  • 待遇面議
Objectives and Scope of Position: Clinical Project Associate is responsible for planning, execution and communication with requesters regarding PAA program (pre-approval access) according to SOPs and local requirements. Primary Responsibilities and Accountabilities: 1. Internal alignment for PAA 2. Receive and evaluate request 3. Liaise with treating physician. 4. Manage UMP process. 5.
一個月以前更新 兩週內11-30人應徵
2019-08-25
科文斯諮詢服務股份有限公司
  • 大學 碩士
  • 二年以上工作經驗
  • 待遇面議
Study startup which include IRB/IEC submission, site selection, recruitment of potential investigators, notifications to regulatory authorities, translation of study-related documentation Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned Study site monitoring including routine monitoring and close-out of clinica
2天以前更新 兩週內11-30人應徵
2019-10-14

Clinical Project Manager

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
  • 五年以上工作經驗
  • 待遇面議
1. Responsible to plan, initiate, develop and organize clinical trials in accordance to the highest standards required in ICH E6 GCP, regulatory compliance, investigator integrity and compliance with the study requirements. 2. Lead and motivate project team(s) on all project-related issues to ensure all activities are conducted in compliance with ICH E6 GCP and applicable local regulatory requirem
2天以前更新 兩週內0-5人應徵
2019-10-14

Clinical Trials Assistant (Taipei)

FULL_TIME
台北市松山區
IQVIA_艾昆緯股份有限公司
  • 大學 碩士
  • 工作經驗不拘
  • 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.
5天以前更新 兩週內大於30人應徵
2019-10-11
臺灣阿斯特捷利康股份有限公司
  • 大學 碩士
  • 四年以上工作經驗
  • 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6-10人應徵
2019-10-08
IQVIA_艾昆緯股份有限公司
  • 大學 碩士
  • 六年以上工作經驗
  • 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
5天以前更新 兩週內0-5人應徵
2019-10-11
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