Live opening · Posted 9 days ago

临床研究助理(Clinical Trial Assistant)

爱恩康临床医学研究(北京)有限公司 · Beijing, Beijing, China (Remote)
Linkedin No
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At a glance

The key details from the original listing.

Posted 9 days ago
Company爱恩康临床医学研究(北京)有限公司
LocationBeijing, Beijing, China (Remote)
Salary8,000 CNY/month - 18K CNY/month
Work modeNo
SourceLinkedin
Listed9 days ago

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About the role

Description supplied by the original job listing.

该职位来源于猎聘 Working fully outsourced at one of our global pharmaceuticalclients, the Clinical Trial Assistant plays a fundamental role in thesuccessful execution of global clinical trials. Operating within the scope ofthe Clinical Development Plan, ICH-GCP guidelines and in accordance with thestudy protocol, local and international regulatory requirements and companyprocedures, the Clinical Trial Assistant (CTA) works to support the completionand coordination of various logistical and administrative tasks. The Clinical Trial Assistant’s (CTA) work is varied,fast-paced and quality focused. Typical duties will include supporting othermembers of the local study team, including Clinical Research Associates andLead Monitors, collecting data required for regulatory submissions, document tracking(contracts, financial agreements, patient informed consent forms, insurancecertificates) and managing the delivery of non-drug related study supplies.Maintaining constructive relationships with site staff (eg Investigators, StudyCoordinators etc) as well as with colleagues within the organisation, theClinical Trial Assistant is responsible for tracking site budget relatedmatters, including processing invoices, tracking payments etc. The maintenanceand updating of the Trial Master File (and preparation for relevant QC checkswhen applicable) also falls within the CTA’s remit. Functioning as a key component of the clinical study team,the Clinical Trials Assistant (CTA) may also be responsible for schedulingmeetings, updating Excel trackers, coordinating the translation of sitedocuments and providing ad-hoc support as appropriate. Requirements To be considered for this position, you must be have adegree (or equivalent) in a relevant life-sciences discipline (nursing, biologyetc) along with previous experience in a similar role, either in apharmaceutical company or a CRO. Fluency in English is essential, along with proficiency inthe use of Microsoft Office suite. Demonstrable experience of working to high quality standardsand resolving issues will also feature in your profile. The ability to effectively communicate with others andfoster positive working relationships will guarantee success within this role

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