職位推薦
- 珍格醫療-臨床銷售 15001-20000
- 地奧制藥-醫藥代表 6001-8000
- 普利德醫療-醫療設備銷售經理 面議
- 大唐-兼職招商經理 面議
- 景德中藥-直營經理 6001-8000
- 安邦醫藥-省區招商經理 8001-10000
- 恒瑞醫藥-醫藥信息溝通專員 6001-8000
- 黃河中藥-學術講師 8001-10000
發布日期:2019-05-19 瀏覽次數:161
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
300多萬優質簡歷
17年行業積淀
2萬多家合作名企業
微信掃一掃 使用小程序