[上海]杭州泰格医药科技股份有限公司

发布日期:2019-05-19 浏览次数:122

公司官网:http://www.tigermed.net
专业1:临床医学与医学技术
专业2:药学
职能类别:临床研究员
职能类别:实习生

岗位要求:

1、临床医学、临床药学、预防医学、药学、护理学等相关专业本科及以上学历;

2、CET6,读写流利;

3、有志于在临床试验行业发展,工作表现优秀有留用机会;

4、此职位面向2019年毕业生,希望每周实习3天以上,持续半年以上。


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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