面議(經常性薪資達4萬元或以上) 台北市中正區 工作經歷不拘 今天剛更新
工作內容
Perform start-up activities in assigned studies, according to applicable regulations, SOPs and work instructions.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Inform team members of completion of regulatory and contractual documents for submission sites.
Distribute completed documents to sites and internal project team members.
Working closely with the Study Start-Up Manager (SSUM), Project Management team, and other departments as necessary.
Support the updating and maintenance of internal database, tracking tools, timelines and project plans with accurate and complete project specific information.
Review, track and follow up the project status, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF).
Review, prepare and negotiate site contracts and budgets with sites.
Other tasks assigned by the supervisor, SSUM
*無經驗可,所需技能由公司培訓。
*有實際做過TFDA /IRB送審工作,且兩年以上工作經驗者優先錄取,待遇從優。
*隨時可報到者優先錄取
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