[上海]杭州泰格醫藥科技股份有限公司

發布日期:2019-05-19 瀏覽次數:161

公司官網:http://www.tigermed.net
專業1:臨床醫學與醫學技術
專業2:藥學
職能類別:臨床研究員
職能類別:實習生

崗位要求:

1、臨床醫學、臨床藥學、預防醫學、藥學、護理學等相關專業本科及以上學歷;

2、CET6,讀寫流利;

3、有志于在臨床試驗行業發展,工作表現優秀有留用機會;

4、此職位面向2019年畢業生,希望每周實習3天以上,持續半年以上。


Responsibilities


(1) Monitoring

Monitoring

- Perform pre-study visit to ensure the site has adequate resources for the study.

- Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined

in protocol, SOP and ICH-GCP.

- Track study recruitment to ensure recruitment target is achieved in all studies.

- Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete

monitoring visit report in a timely manner Coordinating

- Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for

start-up and throughout the study.

- Assemble site specific EC submission dossier, and ensure submission to EC.

Training

- Provide ongoing training to site staff with regards to ICH-GCP, study protocol and requirements.

- Conduct site initiation to ensure that the site has a thorough understanding of the study protocol

and requirements.

Documentation

- Collect essential documents at study start-up, during and at study close-down. Maintain and

update these documents in investigator files, trial master files.

- Prepare/Pack for archiving at the end of the study.

(2) Drug Safety

- Ensure safety information is disseminated to all sites according SOP and applicable regulations.

- Report SAE promptly according to SOPs and applicable regulations.

(3) Finance and Administration

- Finalize budget and obtain signed contract from site, prior to site initiation visit.

- Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(4) Study Tools and system

- Update and maintain Study tools/systems in a timely manner.


Qualifications

Bachelor degree in biomedical/science discipline or equivalent (e.g. medical, Nurse , Pharmacology)

Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/

procedures

Good working and proactive attitude

Value importance of teamwork

Good command of written and verbal English


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